Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8615 |
| ensemblid | ENSG00000138768.15 |
| hgncid | 30904 |
| symbol | USO1 |
| name | USO1 vesicle transport factor |
| refseq_nuc | NM_003715.4 |
| refseq_prot | NP_003706.2 |
| ensembl_nuc | ENST00000514213.7 |
| ensembl_prot | ENSP00000444850.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 75724577 |
| end | 75814286 |
| strand | + |
| ver | v1.2 |
| region | chr4:75724577-75814286 |
| region5000 | chr4:75719577-75819286 |
| regionname0 | USO1_chr4_75724577_75814286 |
| regionname5000 | USO1_chr4_75719577_75819286 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 962 | 277 | 80 | 65 | 78 | 14 | 38 | 66 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0002 | 0/0 | 962 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0003 | 0/0 | 962 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0004 | 0/0 | 962 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0005 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0006 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0007 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| a0008 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | MNFLR others(957): Show |
chr4 | 75719577 | 75819286 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2886 | 107 | 19 | 30 | 37 | 4 | 17 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0002 | 0/0 | 2886 | 86 | 41 | 9 | 25 | 0 | 11 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0003 | 1/0 | 2886 | 42 | 17 | 14 | 1 | 4 | 5 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0004 | 0/1 | 2886 | 31 | 0 | 9 | 12 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0006 | 0/0 | 2886 | 3 | 1 | 0 | 1 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0007 | 0/0 | 2886 | 2 | 0 | 1 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0009 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0010 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0011 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0012 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0014 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0001c0018 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0002c0005 | 0/0 | 2886 | 4 | 0 | 0 | 0 | 0 | 4 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0003c0008 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0004c0019 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0005c0017 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0006c0016 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0007c0015 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 | ||
| a0008c0013 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | ATGAA others(2881): Show |
chr4 | 75719577 | 75819286 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4123 | 105 | 17 | 30 | 37 | 4 | 17 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0001t0003 | 0/0 | 4123 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0002t0001 | 0/0 | 4123 | 83 | 39 | 9 | 25 | 0 | 10 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0002t0002 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0002t0006 | 0/0 | 4123 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0002t0009 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0003t0001 | 0/0 | 4123 | 38 | 16 | 13 | 1 | 4 | 4 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0003t0002 | 1/0 | 4123 | 3 | 1 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0003t0008 | 0/0 | 4123 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0004t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0004t0002 | 0/0 | 4123 | 29 | 0 | 9 | 11 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0004t0005 | 0/1 | 4123 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0006t0001 | 0/0 | 4123 | 3 | 1 | 0 | 1 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0007t0001 | 0/0 | 4123 | 2 | 0 | 1 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0009t0007 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0010t0002 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0011t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0012t0001 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0014t0002 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0001c0018t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0002c0005t0001 | 0/0 | 4123 | 4 | 0 | 0 | 0 | 0 | 4 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0003c0008t0001 | 0/0 | 4123 | 2 | 0 | 0 | 2 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0004c0019t0001 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0005c0017t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0006c0016t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0007c0015t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| a0008c0013t0004 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | CCCTT others(4118): Show |
chr4 | 75719577 | 75819286 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0002g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0008g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0005g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0007t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0009t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0010t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0011t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0012t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0014t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0018t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0003c0008t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0003c0008t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0004c0019t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0005c0017t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0006c0016t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0007c0015t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0008c0013t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0034 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0206 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0009 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0191 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0193 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00323 | hp2 | a0001 | c0004 | t0002 | g0015 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00639 | hp1 | a0001 | c0012 | t0001 | g0054 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00741 | hp1 | a0001 | c0004 | t0002 | g0027 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0201 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0205 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0031 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0013 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0202 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01243 | hp1 | a0001 | c0010 | t0002 | g0006 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0200 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01257 | hp2 | a0004 | c0019 | t0001 | g0059 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0035 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0022 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0215 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0001 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01891 | hp2 | a0005 | c0017 | t0001 | g0162 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0208 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01952 | hp2 | a0001 | c0004 | t0002 | g0033 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0188 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01981 | hp2 | a0001 | c0004 | t0002 | g0029 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0204 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02040 | hp1 | a0001 | c0006 | t0001 | g0216 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0017 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02129 | hp2 | a0001 | c0004 | t0002 | g0008 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02273 | hp1 | a0001 | c0004 | t0002 | g0028 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02886 | hp2 | a0006 | c0016 | t0001 | g0180 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0199 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03017 | hp1 | a0001 | c0004 | t0002 | g0014 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0194 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03098 | hp1 | a0001 | c0009 | t0007 | g0169 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03195 | hp2 | a0001 | c0002 | t0009 | g0159 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03225 | hp1 | a0007 | c0015 | t0001 | g0238 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03225 | hp2 | a0008 | c0013 | t0004 | g0038 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0021 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03453 | hp2 | a0001 | c0014 | t0002 | g0036 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03491 | hp2 | a0002 | c0005 | t0001 | g0224 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0182 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03654 | hp2 | a0002 | c0005 | t0001 | g0222 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03688 | hp1 | a0002 | c0005 | t0001 | g0218 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03704 | hp1 | a0001 | c0004 | t0002 | g0026 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0101 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0228 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0032 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0184 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04115 | hp2 | a0001 | c0003 | t0008 | g0170 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04228 | hp2 | a0002 | c0005 | t0001 | g0221 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18966 | hp1 | a0003 | c0008 | t0001 | g0090 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18966 | hp2 | a0003 | c0008 | t0001 | g0133 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18970 | hp1 | a0001 | c0004 | t0002 | g0024 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18980 | hp1 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18999 | hp1 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0023 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19010 | hp2 | a0001 | c0011 | t0001 | g0103 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19054 | hp1 | a0001 | c0018 | t0001 | g0141 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19057 | hp2 | a0001 | c0004 | t0002 | g0011 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19062 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19081 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19087 | hp1 | a0001 | c0004 | t0002 | g0018 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0187 | EUR | TSI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | GIH | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01123 | hp2 | a0001 | c0007 | t0001 | g0151 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | USA | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | USA | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0005 | g0030 | REF | REF | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0012 | REF | REF | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75771105 | C | G | 1 | a0004 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.523C>G | p.Leu175Val | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/24 | 766/4123 | 523/2889 | 175/962 | chr4 | 75771105 | |||
| chr4:75787081 | C | G | 1 | a0003 | 2 | NA18966.hp1 NA18966.hp2 |
missense_variant | MODERATE | c.875C>G | p.Ser292Cys | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1118/4123 | 875/2889 | 292/962 | chr4 | 75787081 | |||
| chr4:75787185 | G | T | 1 | a0005 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.979G>T | p.Ala327Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1222/4123 | 979/2889 | 327/962 | chr4 | 75787185 | |||
| chr4:75804156 | G | A | 1 | a0002 | 4 | HG03491.hp2 HG03654.hp2 HG03688.hp1 others(1): Show |
missense_variant | MODERATE | c.2009G>A | p.Arg670Lys | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/24 | 2252/4123 | 2009/2889 | 670/962 | chr4 | 75804156 | |||
| chr4:75809026 | A | C | 1 | a0006 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2450A>C | p.Glu817Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2693/4123 | 2450/2889 | 817/962 | chr4 | 75809026 | |||
| chr4:75810432 | G | A | 1 | a0008 | 1 | HG03225.hp2 | missense_variant&splice_region_variant | MODERATE | c.2476G>A | p.Ala826Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/24 | 2719/4123 | 2476/2889 | 826/962 | chr4 | 75810432 | |||
| chr4:75812236 | T | C | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2660T>C | p.Ile887Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/24 | 2903/4123 | 2660/2889 | 887/962 | chr4 | 75812236 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75774678 | C | T | 1 | a0001c0018 | 1 | NA19054.hp1 | splice_region_variant&synonymous_variant | LOW | c.558C>T | p.Gly186Gly | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/24 | 801/4123 | 558/2889 | 186/962 | chr4 | 75774678 | |||
| chr4:75774774 | A | G | 1 | a0001c0006 | 3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.654A>G | p.Ser218Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/24 | 897/4123 | 654/2889 | 218/962 | chr4 | 75774774 | |||
| chr4:75787172 | T | A | 1 | a0001c0009 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.966T>A | p.Ala322Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1209/4123 | 966/2889 | 322/962 | chr4 | 75787172 | |||
| chr4:75790766 | C | T | 1 | a0001c0009 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1209C>T | p.Ile403Ile | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/24 | 1452/4123 | 1209/2889 | 403/962 | chr4 | 75790766 | |||
| chr4:75799732 | T | C | 15 | a0001c0001 a0001c0002 a0001c0007 others(12): Show |
211 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(208): Show |
splice_region_variant&synonymous_variant | LOW | c.1563T>C | p.Phe521Phe | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/24 | 1806/4123 | 1563/2889 | 521/962 | chr4 | 75799732 | |||
| chr4:75800431 | G | A | 1 | a0001c0007 | 2 | HG01123.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.1644G>A | p.Ser548Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/24 | 1887/4123 | 1644/2889 | 548/962 | chr4 | 75800431 | |||
| chr4:75801200 | G | A | 11 | a0001c0001 a0001c0004 a0001c0007 others(8): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
splice_region_variant&synonymous_variant | LOW | c.1986G>A | p.Gln662Gln | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/24 | 2229/4123 | 1986/2889 | 662/962 | chr4 | 75801200 | |||
| chr4:75805294 | T | C | 1 | a0001c0010 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2280T>C | p.Ile760Ile | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/24 | 2523/4123 | 2280/2889 | 760/962 | chr4 | 75805294 | |||
| chr4:75806548 | T | A | 1 | a0001c0011 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.2352T>A | p.Ser784Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/24 | 2595/4123 | 2352/2889 | 784/962 | chr4 | 75806548 | |||
| chr4:75809042 | A | G | 2 | a0001c0004 a0001c0014 |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
synonymous_variant | LOW | c.2466A>G | p.Thr822Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2709/4123 | 2466/2889 | 822/962 | chr4 | 75809042 | |||
| chr4:75809048 | G | A | 1 | a0001c0012 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.2472G>A | p.Ala824Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2715/4123 | 2472/2889 | 824/962 | chr4 | 75809048 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75724680 | G | A | 1 | a0008c0013t0004 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 140 | chr4 | 75724680 | ||||||
| chr4:75724709 | C | A | 1 | a0001c0001t0003 | 2 | HG02109.hp1 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-111C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 111 | chr4 | 75724709 | ||||||
| chr4:75724740 | C | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(18): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
5_prime_UTR_variant | MODIFIER | c.-80C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 80 | chr4 | 75724740 | ||||||
| chr4:75813396 | T | G | 1 | a0001c0002t0006 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 101 | chr4 | 75813396 | ||||||
| chr4:75813741 | T | G | 1 | a0001c0009t0007 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 446 | chr4 | 75813741 | ||||||
| chr4:75814185 | T | A | 1 | a0001c0003t0008 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 890 | chr4 | 75814185 | ||||||
| chr4:75814224 | T | C | 1 | a0001c0002t0009 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*929T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 929 | chr4 | 75814224 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75724992 | C | G | 251 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(248): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.66+107C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75724992 | |||||||
| chr4:75725099 | C | A | 1 | a0001c0002t0001g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+214C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725099 | |||||||
| chr4:75725222 | C | T | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.66+337C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725222 | |||||||
| chr4:75725259 | C | T | 250 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(247): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+374C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725259 | |||||||
| chr4:75725588 | C | T | 135 | a0001c0001t0001g0179 a0001c0001t0001g0217 a0001c0002t0001g0037 others(132): Show |
136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.66+703C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725588 | |||||||
| chr4:75725617 | T | TA | 114 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(111): Show |
114 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.66+747dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75725617 | ||||||
| chr4:75725806 | T | C | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.66+921T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725806 | |||||||
| chr4:75726169 | C | T | 250 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(247): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+1284C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726169 | |||||||
| chr4:75726195 | C | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+1310C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726195 | |||||||
| chr4:75726220 | A | ACGGTGAG others(7): Show |
6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+1338_66+1351dup others(14): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726220 | ||||||
| chr4:75726281 | C | CA | 114 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.66+1416dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | ||||||
| chr4:75726281 | C | CAA | 24 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.66+1415_66+1416dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | ||||||
| chr4:75726281 | CA | C | 6 | a0001c0001t0001g0140 a0001c0002t0002g0005 a0001c0003t0002g0003 others(3): Show |
6 | HG01069.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+1416delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | ||||||
| chr4:75726293 | AAAAAAAA others(57): Show |
A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01175.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.66+1411_66+1474del others(64): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726293 | ||||||
| chr4:75726301 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0119 others(1): Show |
4 | HG01943.hp1 HG02293.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+1416A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726301 | |||||||
| chr4:75726567 | C | CA | 111 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.66+1696dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726567 | ||||||
| chr4:75726797 | C | G | 72 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(69): Show |
72 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+1912C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726797 | |||||||
| chr4:75726849 | T | C | 1 | a0001c0003t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.66+1964T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726849 | |||||||
| chr4:75727126 | T | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+2241T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727126 | |||||||
| chr4:75727205 | T | G | 250 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(247): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+2320T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727205 | |||||||
| chr4:75727842 | C | T | 1 | a0001c0007t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.66+2957C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727842 | |||||||
| chr4:75727953 | T | TA | 114 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(111): Show |
114 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.66+3071dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75727953 | ||||||
| chr4:75728106 | C | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+3221C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728106 | |||||||
| chr4:75728199 | A | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+3314A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728199 | |||||||
| chr4:75728257 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.66+3372G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728257 | |||||||
| chr4:75728388 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+3503C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728388 | |||||||
| chr4:75728553 | G | A | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+3668G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728553 | |||||||
| chr4:75728859 | C | T | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+3974C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728859 | |||||||
| chr4:75728895 | T | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4010T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728895 | |||||||
| chr4:75728958 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+4073C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728958 | |||||||
| chr4:75729088 | A | G | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+4203A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729088 | |||||||
| chr4:75729139 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66+4254A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729139 | |||||||
| chr4:75729286 | A | T | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.66+4401A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729286 | |||||||
| chr4:75729365 | A | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+4480A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729365 | |||||||
| chr4:75729465 | G | A | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.66+4580G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729465 | |||||||
| chr4:75729484 | T | C | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+4599T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729484 | |||||||
| chr4:75729737 | A | C | 2 | a0001c0006t0001g0215 a0001c0006t0001g0216 |
2 | HG01516.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.66+4852A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729737 | |||||||
| chr4:75729803 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+4918T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729803 | |||||||
| chr4:75730097 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0134 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.66+5212A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730097 | |||||||
| chr4:75730361 | A | C | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.66+5476A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730361 | |||||||
| chr4:75730577 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+5692C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730577 | |||||||
| chr4:75730640 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+5755A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730640 | |||||||
| chr4:75730822 | T | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+5937T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730822 | |||||||
| chr4:75731002 | C | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+6117C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731002 | |||||||
| chr4:75731362 | G | A | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+6477G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731362 | |||||||
| chr4:75731444 | C | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.66+6559C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731444 | |||||||
| chr4:75731488 | C | G | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+6603C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731488 | |||||||
| chr4:75731561 | CA | C | 241 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(238): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.66+6691delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75731561 | ||||||
| chr4:75731709 | C | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.66+6824C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731709 | |||||||
| chr4:75731975 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+7090G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731975 | |||||||
| chr4:75731983 | G | A | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+7098G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731983 | |||||||
| chr4:75732052 | A | G | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.66+7167A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732052 | |||||||
| chr4:75732207 | G | A | 1 | a0001c0004t0002g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.66+7322G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732207 | |||||||
| chr4:75732260 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+7375T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732260 | |||||||
| chr4:75732271 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+7386G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732271 | |||||||
| chr4:75732315 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.66+7430T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732315 | |||||||
| chr4:75732320 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+7435T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732320 | |||||||
| chr4:75732374 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+7489A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732374 | |||||||
| chr4:75732443 | A | C | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+7558A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732443 | |||||||
| chr4:75732666 | G | C | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.66+7781G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732666 | |||||||
| chr4:75732675 | A | G | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+7790A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732675 | |||||||
| chr4:75732771 | T | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66+7886T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732771 | |||||||
| chr4:75732835 | C | T | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.66+7950C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732835 | |||||||
| chr4:75732876 | T | TAAAA | 8 | a0001c0002t0001g0153 a0001c0002t0001g0176 a0001c0002t0001g0280 others(5): Show |
8 | HG01168.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+8010_66+8013dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAA | 106 | a0001c0001t0001g0040 a0001c0001t0001g0145 a0001c0001t0001g0146 others(103): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.66+8009_66+8013dup others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAA | 29 | a0001c0001t0001g0039 a0001c0001t0001g0144 a0001c0001t0001g0179 others(26): Show |
29 | HG00609.hp2 HG01261.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.66+8008_66+8013dup others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAAA | 61 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0047 others(58): Show |
61 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.66+8007_66+8013dup others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAAA others(1): Show |
40 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(37): Show |
40 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.66+8006_66+8013dup others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAAA others(2): Show |
6 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0055 others(3): Show |
6 | HG00438.hp2 HG01361.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+8005_66+8013dup others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAAA others(3): Show |
1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.66+8004_66+8013dup others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732876 | T | TAAAAAAA others(6): Show |
2 | a0001c0012t0001g0054 a0008c0013t0004g0038 |
2 | HG00639.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.66+8001_66+8013dup others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | ||||||
| chr4:75732918 | T | A | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+8033T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732918 | |||||||
| chr4:75733031 | C | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+8146C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733031 | |||||||
| chr4:75733088 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.66+8203G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733088 | |||||||
| chr4:75733133 | C | T | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.66+8248C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733133 | |||||||
| chr4:75733208 | G | A | 6 | a0001c0003t0001g0185 a0001c0003t0001g0209 a0001c0003t0001g0210 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+8323G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733208 | |||||||
| chr4:75733246 | G | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
12 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+8361G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733246 | |||||||
| chr4:75733271 | A | T | 3 | a0001c0002t0001g0235 a0001c0002t0001g0278 a0001c0002t0001g0279 |
3 | HG01358.hp2 HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.66+8386A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733271 | |||||||
| chr4:75733327 | C | G | 3 | a0001c0002t0001g0219 a0001c0002t0001g0223 a0002c0005t0001g0224 |
3 | HG02738.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.66+8442C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733327 | |||||||
| chr4:75733522 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+8637G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733522 | |||||||
| chr4:75733556 | C | G | 1 | a0001c0004t0002g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.66+8671C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733556 | |||||||
| chr4:75733792 | C | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.66+8907C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733792 | |||||||
| chr4:75733924 | T | G | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+9039T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733924 | |||||||
| chr4:75733935 | A | AT | 15 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0179 others(12): Show |
15 | HG00741.hp1 HG01109.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.66+9076dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | ||||||
| chr4:75733935 | AT | A | 62 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(59): Show |
63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.66+9076delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | ||||||
| chr4:75733935 | ATT | A | 83 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.66+9075_66+9076del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | ||||||
| chr4:75733935 | ATTTTTTT others(1): Show |
A | 70 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(67): Show |
70 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.66+9069_66+9076del others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | ||||||
| chr4:75734234 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+9349A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734234 | |||||||
| chr4:75734298 | G | C | 1 | a0001c0003t0001g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.66+9413G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734298 | |||||||
| chr4:75734312 | A | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+9427A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734312 | |||||||
| chr4:75734703 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01175.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.66+9818C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734703 | |||||||
| chr4:75734718 | C | CT | 16 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(13): Show |
16 | HG00140.hp2 HG01109.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+9861dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | C | CTT | 67 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0069 others(64): Show |
68 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.66+9860_66+9861dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | C | CTTT | 92 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0051 others(89): Show |
92 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.66+9859_66+9861dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | C | CTTTT | 57 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(54): Show |
57 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.66+9858_66+9861dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | C | CTTTTT | 22 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0067 others(19): Show |
22 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.66+9857_66+9861dup others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.66+9852_66+9861del others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734718 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.66+9851_66+9861del others(11): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | ||||||
| chr4:75734865 | A | T | 4 | a0001c0004t0002g0018 a0001c0004t0002g0023 a0001c0004t0002g0024 others(1): Show |
4 | NA18970.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+9980A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734865 | |||||||
| chr4:75735125 | C | A | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+10240C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735125 | |||||||
| chr4:75735316 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+10431A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735316 | |||||||
| chr4:75735715 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.66+10830C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735715 | |||||||
| chr4:75735721 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+10836A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735721 | |||||||
| chr4:75735924 | A | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11039A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735924 | |||||||
| chr4:75736250 | G | A | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+11365G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736250 | |||||||
| chr4:75736307 | C | CT | 29 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(26): Show |
29 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.66+11450dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | ||||||
| chr4:75736307 | C | CTT | 11 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0063 others(8): Show |
11 | HG00438.hp2 HG01517.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+11449_66+11450d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | ||||||
| chr4:75736307 | CTT | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0146 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+11449_66+11450d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | ||||||
| chr4:75736307 | CTTT | C | 12 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0156 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+11448_66+11450d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | ||||||
| chr4:75736307 | CTTTT | C | 120 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0157 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.66+11447_66+11450d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | ||||||
| chr4:75736362 | G | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+11477G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736362 | |||||||
| chr4:75736431 | C | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+11546C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736431 | |||||||
| chr4:75736659 | G | A | 3 | a0001c0003t0002g0003 a0001c0003t0002g0004 a0001c0009t0007g0169 |
3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.66+11774G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736659 | |||||||
| chr4:75736758 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11873T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736758 | |||||||
| chr4:75736889 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0121 |
3 | NA18949.hp1 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.66+12004T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736889 | |||||||
| chr4:75737018 | T | A | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+12133T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737018 | |||||||
| chr4:75737057 | G | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | NA18962.hp2 NA18966.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+12172G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737057 | |||||||
| chr4:75737111 | T | A | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+12226T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737111 | |||||||
| chr4:75737153 | A | G | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+12268A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737153 | |||||||
| chr4:75737281 | AT | A | 3 | a0001c0006t0001g0199 a0001c0006t0001g0215 a0001c0006t0001g0216 |
3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+12397delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737281 | |||||||
| chr4:75737485 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12600A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737485 | |||||||
| chr4:75737547 | G | GA | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+12663dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75737547 | ||||||
| chr4:75737761 | T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66+12876T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737761 | |||||||
| chr4:75737816 | C | CATT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+12950_66+12952d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75737816 | ||||||
| chr4:75737884 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12999G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737884 | |||||||
| chr4:75737951 | C | T | 7 | a0001c0002t0001g0231 a0001c0002t0001g0259 a0001c0002t0001g0260 others(4): Show |
7 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+13066C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737951 | |||||||
| chr4:75738139 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+13254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738139 | |||||||
| chr4:75738188 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0119 |
3 | HG01943.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.66+13303A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738188 | |||||||
| chr4:75738241 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+13356A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738241 | |||||||
| chr4:75738389 | G | A | 13 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(10): Show |
13 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+13504G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738389 | |||||||
| chr4:75738456 | CA | C | 72 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(69): Show |
72 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+13583delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75738456 | ||||||
| chr4:75738539 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0002g0005 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.66+13654G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738539 | |||||||
| chr4:75738731 | T | C | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.67-13642T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738731 | |||||||
| chr4:75738795 | A | T | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.67-13578A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738795 | |||||||
| chr4:75738865 | T | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13508T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738865 | |||||||
| chr4:75738955 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13418C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738955 | |||||||
| chr4:75738977 | C | G | 1 | a0001c0003t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67-13396C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738977 | |||||||
| chr4:75738998 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-13375G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738998 | |||||||
| chr4:75739001 | C | T | 76 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(73): Show |
76 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.67-13372C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739001 | |||||||
| chr4:75739002 | G | GC | 3 | a0001c0003t0002g0003 a0001c0003t0002g0004 a0001c0009t0007g0169 |
3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13369dupC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739002 | ||||||
| chr4:75739095 | G | A | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13278G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739095 | |||||||
| chr4:75739098 | C | T | 10 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0267 others(7): Show |
10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-13275C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739098 | |||||||
| chr4:75739099 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13274G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739099 | |||||||
| chr4:75739104 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13269G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739104 | |||||||
| chr4:75739105 | T | G | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.67-13268T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739105 | |||||||
| chr4:75739144 | G | T | 1 | a0001c0006t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-13229G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739144 | |||||||
| chr4:75739376 | T | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-12997T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739376 | |||||||
| chr4:75739403 | C | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-12970C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739403 | |||||||
| chr4:75739538 | C | CT | 100 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(97): Show |
100 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.67-12815dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | ||||||
| chr4:75739538 | C | CTT | 10 | a0001c0001t0001g0041 a0001c0001t0001g0056 a0001c0001t0001g0071 others(7): Show |
10 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-12816_67-12815d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | ||||||
| chr4:75739538 | CT | C | 16 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(13): Show |
16 | HG01099.hp1 HG01257.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-12815delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | ||||||
| chr4:75739544 | T | C | 4 | a0001c0002t0001g0220 a0002c0005t0001g0218 a0002c0005t0001g0221 others(1): Show |
4 | HG03491.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-12829T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739544 | |||||||
| chr4:75739708 | A | G | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-12665A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739708 | |||||||
| chr4:75739807 | T | C | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-12566T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739807 | |||||||
| chr4:75739813 | G | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-12560G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739813 | |||||||
| chr4:75739910 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-12463T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739910 | |||||||
| chr4:75739922 | A | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-12451A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739922 | |||||||
| chr4:75739963 | T | C | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-12410T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739963 | |||||||
| chr4:75739989 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-12384T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739989 | |||||||
| chr4:75740074 | A | G | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.67-12299A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740074 | |||||||
| chr4:75740450 | G | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-11923G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740450 | |||||||
| chr4:75740733 | A | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-11640A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740733 | |||||||
| chr4:75740819 | G | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0089 others(2): Show |
5 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-11554G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740819 | |||||||
| chr4:75740897 | G | A | 1 | a0001c0002t0001g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-11476G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740897 | |||||||
| chr4:75740928 | A | G | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-11445A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740928 | |||||||
| chr4:75740941 | T | C | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-11432T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740941 | |||||||
| chr4:75741094 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11279G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741094 | |||||||
| chr4:75741285 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.67-11088A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741285 | |||||||
| chr4:75741536 | G | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-10837G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741536 | |||||||
| chr4:75741596 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0087 |
3 | HG00140.hp1 HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.67-10777T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741596 | |||||||
| chr4:75741601 | CT | C | 213 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(210): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.67-10749delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75741601 | ||||||
| chr4:75741601 | CTT | C | 14 | a0001c0001t0001g0093 a0001c0001t0001g0126 a0001c0002t0001g0239 others(11): Show |
14 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-10750_67-10749d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75741601 | ||||||
| chr4:75741661 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-10712A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741661 | |||||||
| chr4:75741891 | G | A | 3 | a0001c0002t0001g0243 a0001c0002t0001g0244 a0001c0002t0006g0228 |
3 | HG03669.hp2 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.67-10482G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741891 | |||||||
| chr4:75741984 | C | T | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67-10389C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741984 | |||||||
| chr4:75742004 | C | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10369C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742004 | |||||||
| chr4:75742060 | T | G | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.67-10313T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742060 | |||||||
| chr4:75742078 | A | G | 3 | a0001c0006t0001g0199 a0001c0006t0001g0215 a0001c0006t0001g0216 |
3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-10295A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742078 | |||||||
| chr4:75742110 | T | C | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67-10263T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742110 | |||||||
| chr4:75742181 | G | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67-10192G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742181 | |||||||
| chr4:75742280 | C | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-10093C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742280 | |||||||
| chr4:75742414 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.67-9959C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742414 | |||||||
| chr4:75742443 | A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9930A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742443 | |||||||
| chr4:75742478 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0122 |
2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.67-9895G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742478 | |||||||
| chr4:75742525 | C | T | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-9848C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742525 | |||||||
| chr4:75742893 | C | T | 1 | a0007c0015t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-9480C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742893 | |||||||
| chr4:75742913 | G | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9460G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742913 | |||||||
| chr4:75742969 | A | G | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-9404A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742969 | |||||||
| chr4:75742985 | C | CT | 44 | a0001c0001t0001g0076 a0001c0001t0001g0114 a0001c0001t0001g0121 others(41): Show |
45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.67-9371dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75742985 | ||||||
| chr4:75742999 | T | A | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-9374T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742999 | |||||||
| chr4:75743083 | C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9290C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743083 | |||||||
| chr4:75743390 | A | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-8983A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743390 | |||||||
| chr4:75743507 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-8866T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743507 | |||||||
| chr4:75743553 | A | G | 4 | a0001c0003t0001g0182 a0001c0003t0001g0183 a0001c0003t0001g0184 others(1): Show |
4 | HG03654.hp1 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-8820A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743553 | |||||||
| chr4:75743593 | G | T | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.67-8780G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743593 | |||||||
| chr4:75743643 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67-8730C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743643 | |||||||
| chr4:75743790 | T | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-8583T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743790 | |||||||
| chr4:75743822 | G | C | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-8551G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743822 | |||||||
| chr4:75743862 | C | T | 7 | a0001c0004t0002g0009 a0001c0004t0002g0014 a0001c0004t0002g0028 others(4): Show |
7 | HG00140.hp2 HG01346.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-8511C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743862 | |||||||
| chr4:75744061 | C | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-8312C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744061 | |||||||
| chr4:75744307 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0179 |
3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.67-8066C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744307 | |||||||
| chr4:75744354 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-8019G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744354 | |||||||
| chr4:75744443 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-7930G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744443 | |||||||
| chr4:75744669 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67-7704C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744669 | |||||||
| chr4:75744676 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0085 |
2 | NA18994.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.67-7697T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744676 | |||||||
| chr4:75744829 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-7544A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744829 | |||||||
| chr4:75744996 | T | C | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-7377T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744996 | |||||||
| chr4:75745119 | C | T | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.67-7254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745119 | |||||||
| chr4:75745212 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67-7161T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745212 | |||||||
| chr4:75745212 | T | TTA | 4 | a0001c0002t0001g0239 a0001c0002t0001g0240 a0001c0002t0001g0241 others(1): Show |
4 | HG01884.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7148_67-7147dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75745212 | ||||||
| chr4:75745312 | G | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-7061G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745312 | |||||||
| chr4:75745505 | T | C | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.67-6868T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745505 | |||||||
| chr4:75745514 | C | T | 8 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0229 others(5): Show |
8 | NA18941.hp2 NA18950.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-6859C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745514 | |||||||
| chr4:75745729 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.67-6644G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745729 | |||||||
| chr4:75745775 | TTG | T | 90 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(87): Show |
90 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.67-6596_67-6595del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75745775 | ||||||
| chr4:75745798 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-6575G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745798 | |||||||
| chr4:75745922 | G | A | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-6451G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745922 | |||||||
| chr4:75745985 | A | C | 8 | a0001c0002t0001g0225 a0001c0002t0001g0232 a0001c0002t0001g0237 others(5): Show |
8 | HG00609.hp2 NA18940.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-6388A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745985 | |||||||
| chr4:75746221 | A | G | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-6152A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75746221 | |||||||
| chr4:75746886 | G | T | 1 | a0001c0002t0001g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-5487G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75746886 | |||||||
| chr4:75747005 | T | C | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-5368T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747005 | |||||||
| chr4:75747065 | A | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5308A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747065 | |||||||
| chr4:75747270 | C | A | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.67-5103C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747270 | |||||||
| chr4:75747602 | C | CT | 16 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(13): Show |
16 | HG01168.hp2 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.67-4746dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | ||||||
| chr4:75747602 | CT | C | 86 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(83): Show |
86 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.67-4746delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | ||||||
| chr4:75747602 | CTT | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0144 a0001c0001t0001g0146 others(21): Show |
24 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.67-4747_67-4746del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | ||||||
| chr4:75747620 | T | C | 25 | a0001c0004t0001g0049 a0001c0004t0002g0007 a0001c0004t0002g0008 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.67-4753T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747620 | |||||||
| chr4:75747696 | G | A | 158 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.67-4677G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747696 | |||||||
| chr4:75747787 | T | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-4586T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747787 | |||||||
| chr4:75747900 | C | CT | 19 | a0001c0002t0001g0156 a0001c0002t0001g0163 a0001c0002t0001g0226 others(16): Show |
19 | HG01168.hp1 HG01346.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-4449dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747900 | ||||||
| chr4:75747900 | CT | C | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(114): Show |
117 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.67-4449delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747900 | ||||||
| chr4:75748019 | T | A | 1 | a0001c0002t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67-4354T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748019 | |||||||
| chr4:75748065 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.67-4308G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748065 | |||||||
| chr4:75748095 | C | T | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-4278C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748095 | |||||||
| chr4:75748123 | C | G | 42 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(39): Show |
43 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.67-4250C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748123 | |||||||
| chr4:75748181 | G | A | 44 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(41): Show |
45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.67-4192G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748181 | |||||||
| chr4:75748201 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-4172G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748201 | |||||||
| chr4:75748211 | C | CT | 8 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(5): Show |
8 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-4144dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748211 | ||||||
| chr4:75748211 | C | CTT | 106 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.67-4145_67-4144dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748211 | ||||||
| chr4:75748353 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.67-4020T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748353 | |||||||
| chr4:75748366 | T | C | 73 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(70): Show |
73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.67-4007T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748366 | |||||||
| chr4:75748441 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-3932A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748441 | |||||||
| chr4:75748445 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-3928T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748445 | |||||||
| chr4:75748497 | G | C | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3876G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748497 | |||||||
| chr4:75748524 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-3849A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748524 | |||||||
| chr4:75748554 | T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-3819T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748554 | |||||||
| chr4:75748752 | C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-3621C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748752 | |||||||
| chr4:75748854 | T | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-3519T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748854 | |||||||
| chr4:75748944 | T | TA | 27 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.67-3421dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748944 | ||||||
| chr4:75748951 | A | AT | 5 | a0001c0004t0002g0011 a0001c0004t0002g0017 a0001c0014t0002g0036 others(2): Show |
5 | HG02074.hp2 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3422_67-3421ins others(1): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748951 | |||||||
| chr4:75749115 | T | G | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.67-3258T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749115 | |||||||
| chr4:75749404 | G | T | 242 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(239): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.67-2969G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749404 | |||||||
| chr4:75749459 | G | C | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-2914G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749459 | |||||||
| chr4:75749700 | A | G | 2 | a0001c0004t0002g0011 a0001c0004t0002g0017 |
2 | HG02074.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.67-2673A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749700 | |||||||
| chr4:75749713 | C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-2660C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749713 | |||||||
| chr4:75749822 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-2551G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749822 | |||||||
| chr4:75750247 | A | G | 1 | a0001c0003t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-2126A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750247 | |||||||
| chr4:75750278 | A | G | 1 | a0001c0002t0001g0247 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-2095A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750278 | |||||||
| chr4:75750367 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2006G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750367 | |||||||
| chr4:75750433 | A | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1940A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750433 | |||||||
| chr4:75750517 | C | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1856C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750517 | |||||||
| chr4:75750562 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.67-1811C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750562 | |||||||
| chr4:75750603 | C | A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1770C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750603 | |||||||
| chr4:75750707 | TCTCTTGA others(23): Show |
T | 82 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(79): Show |
82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.67-1662_67-1633del others(30): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75750707 | ||||||
| chr4:75750761 | G | A | 2 | a0001c0003t0001g0189 a0001c0003t0001g0203 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.67-1612G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750761 | |||||||
| chr4:75750772 | C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1601C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750772 | |||||||
| chr4:75750784 | A | G | 1 | a0001c0003t0001g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-1589A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750784 | |||||||
| chr4:75750896 | C | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-1477C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750896 | |||||||
| chr4:75750930 | A | G | 83 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(80): Show |
83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.67-1443A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750930 | |||||||
| chr4:75750948 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0058 |
2 | HG00438.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.67-1425C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750948 | |||||||
| chr4:75751129 | A | G | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-1244A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751129 | |||||||
| chr4:75751185 | ATTATT | A | 30 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.67-1165_67-1161del others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75751185 | ||||||
| chr4:75751235 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1138G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751235 | |||||||
| chr4:75751372 | C | T | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.67-1001C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751372 | |||||||
| chr4:75751557 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-816G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751557 | |||||||
| chr4:75751578 | C | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-795C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751578 | |||||||
| chr4:75751688 | A | G | 1 | a0001c0003t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67-685A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751688 | |||||||
| chr4:75751729 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.67-644G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751729 | |||||||
| chr4:75751763 | C | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-610C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751763 | |||||||
| chr4:75751773 | A | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-600A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751773 | |||||||
| chr4:75751798 | C | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-575C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751798 | |||||||
| chr4:75751828 | G | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-545G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751828 | |||||||
| chr4:75752030 | T | TA | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-342dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75752030 | ||||||
| chr4:75752040 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-333A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75752040 | |||||||
| chr4:75752338 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0087 |
2 | HG00140.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.67-35T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75752338 | |||||||
| chr4:75752480 | T | C | 1 | a0001c0002t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+21T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 2/23 | chr4 | 75752480 | |||||||
| chr4:75752488 | T | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+29T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 2/23 | chr4 | 75752488 | |||||||
| chr4:75753040 | TA | T | 73 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(70): Show |
73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.218+437delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753040 | |||||||
| chr4:75753124 | G | A | 108 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.218+520G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753124 | |||||||
| chr4:75753217 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+613G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753217 | |||||||
| chr4:75753285 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.218+681G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753285 | |||||||
| chr4:75753347 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+743A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753347 | |||||||
| chr4:75753360 | C | T | 31 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.218+756C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753360 | |||||||
| chr4:75753371 | AAAAATAA others(1): Show |
A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.218+772_218+779del others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753371 | ||||||
| chr4:75753439 | T | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.218+835T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753439 | |||||||
| chr4:75753495 | A | G | 1 | a0001c0002t0001g0236 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.218+891A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753495 | |||||||
| chr4:75753668 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1064T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753668 | |||||||
| chr4:75753669 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1065G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753669 | |||||||
| chr4:75753780 | A | AT | 70 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 others(67): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.218+1197dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753780 | ||||||
| chr4:75753780 | AT | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0125 others(6): Show |
9 | HG01884.hp2 HG02004.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+1197delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753780 | ||||||
| chr4:75753814 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+1210C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753814 | |||||||
| chr4:75754047 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+1443A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754047 | |||||||
| chr4:75754086 | C | CT | 37 | a0001c0001t0001g0055 a0001c0002t0001g0229 a0001c0002t0001g0257 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.218+1495dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75754086 | ||||||
| chr4:75754086 | CT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0102 others(3): Show |
6 | HG01975.hp1 HG02004.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1495delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75754086 | ||||||
| chr4:75754139 | A | G | 1 | a0001c0004t0002g0020 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.218+1535A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754139 | |||||||
| chr4:75754147 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1543G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754147 | |||||||
| chr4:75754168 | T | C | 263 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(260): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.218+1564T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754168 | |||||||
| chr4:75754232 | C | T | 1 | a0001c0003t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218+1628C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754232 | |||||||
| chr4:75754605 | C | T | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+2001C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754605 | |||||||
| chr4:75754606 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.218+2002G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754606 | |||||||
| chr4:75754739 | A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+2135A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754739 | |||||||
| chr4:75754832 | G | T | 14 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0178 others(11): Show |
15 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.218+2228G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754832 | |||||||
| chr4:75755098 | T | C | 1 | a0001c0004t0002g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.219-2399T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755098 | |||||||
| chr4:75755123 | T | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219-2374T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755123 | |||||||
| chr4:75755124 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-2373A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755124 | |||||||
| chr4:75755311 | T | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-2186T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755311 | |||||||
| chr4:75755322 | G | A | 144 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(141): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.219-2175G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755322 | |||||||
| chr4:75755529 | C | T | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219-1968C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755529 | |||||||
| chr4:75755810 | C | A | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219-1687C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755810 | |||||||
| chr4:75756077 | G | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-1420G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756077 | |||||||
| chr4:75756126 | C | T | 1 | a0001c0003t0001g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.219-1371C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756126 | |||||||
| chr4:75756143 | C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.219-1354C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756143 | |||||||
| chr4:75756169 | C | CA | 124 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(121): Show |
124 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.219-1312dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756169 | ||||||
| chr4:75756292 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0087 |
2 | HG00140.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.219-1205A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756292 | |||||||
| chr4:75756347 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.219-1150G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756347 | |||||||
| chr4:75756362 | T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-1135T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756362 | |||||||
| chr4:75756417 | TATAAA | T | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-1079_219-1075d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756417 | |||||||
| chr4:75756507 | A | AT | 136 | a0001c0001t0001g0102 a0001c0002t0001g0037 a0001c0002t0001g0152 others(133): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.219-974dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756507 | ||||||
| chr4:75756507 | A | ATT | 114 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(111): Show |
114 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.219-975_219-974dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756507 | ||||||
| chr4:75756585 | C | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-912C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756585 | |||||||
| chr4:75756586 | A | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-911A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756586 | |||||||
| chr4:75756589 | C | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-908C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756589 | |||||||
| chr4:75756590 | T | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-907T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756590 | |||||||
| chr4:75756592 | T | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-905T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756592 | |||||||
| chr4:75756595 | C | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-902C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756595 | |||||||
| chr4:75756632 | G | A | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.219-865G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756632 | |||||||
| chr4:75756636 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.219-861A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756636 | |||||||
| chr4:75756706 | G | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-791G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756706 | |||||||
| chr4:75756746 | C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.219-751C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756746 | |||||||
| chr4:75756764 | C | T | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.219-733C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756764 | |||||||
| chr4:75756769 | T | C | 1 | a0001c0002t0001g0231 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.219-728T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756769 | |||||||
| chr4:75756863 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.219-634A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756863 | |||||||
| chr4:75756958 | C | CAT | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.219-531_219-530dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756958 | ||||||
| chr4:75756984 | C | T | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-513C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756984 | |||||||
| chr4:75757112 | A | G | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-385A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757112 | |||||||
| chr4:75757116 | A | ACT | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-380_219-379dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75757116 | ||||||
| chr4:75757175 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219-322T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757175 | |||||||
| chr4:75757423 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-74A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757423 | |||||||
| chr4:75757622 | G | A | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295+49G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75757622 | |||||||
| chr4:75757790 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295+217A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75757790 | |||||||
| chr4:75758066 | C | T | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+493C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758066 | |||||||
| chr4:75758306 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.295+733C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758306 | |||||||
| chr4:75758543 | A | T | 5 | a0001c0004t0002g0010 a0001c0004t0002g0015 a0001c0004t0002g0022 others(2): Show |
5 | HG00323.hp2 HG00741.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+970A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758543 | |||||||
| chr4:75758579 | C | T | 73 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(70): Show |
73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+1006C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758579 | |||||||
| chr4:75758729 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.295+1156A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758729 | |||||||
| chr4:75758903 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1330C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758903 | |||||||
| chr4:75759107 | G | A | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+1534G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759107 | |||||||
| chr4:75759245 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1672C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759245 | |||||||
| chr4:75759246 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0093 others(5): Show |
8 | HG01069.hp1 HG01099.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+1684_295+1691d others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(2): Show |
80 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(77): Show |
80 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.295+1683_295+1691d others(11): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(3): Show |
16 | a0001c0001t0001g0041 a0001c0001t0001g0076 a0001c0001t0001g0086 others(13): Show |
16 | HG00280.hp1 HG01943.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.295+1682_295+1691d others(12): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0074 a0001c0001t0001g0089 a0001c0001t0001g0106 others(3): Show |
6 | HG02300.hp1 HG02886.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1681_295+1691d others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0001g0172 a0001c0002t0001g0177 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.295+1679_295+1691d others(15): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295+1678_295+1691d others(16): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(8): Show |
10 | a0001c0002t0001g0171 a0001c0002t0001g0176 a0001c0003t0001g0002 others(7): Show |
11 | HG00099.hp2 HG02074.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+1677_295+1691d others(17): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(9): Show |
31 | a0001c0002t0001g0157 a0001c0002t0001g0165 a0001c0002t0001g0167 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.295+1676_295+1691d others(18): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(10): Show |
33 | a0001c0002t0001g0153 a0001c0002t0001g0158 a0001c0002t0001g0166 others(30): Show |
33 | HG00733.hp2 HG01261.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+1675_295+1691d others(19): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(11): Show |
23 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0160 others(20): Show |
23 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+1674_295+1691d others(20): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(12): Show |
14 | a0001c0001t0001g0040 a0001c0001t0001g0179 a0001c0002t0001g0156 others(11): Show |
14 | HG02129.hp1 HG02145.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0039 a0001c0002t0001g0152 a0001c0002t0001g0225 others(5): Show |
8 | HG00609.hp2 HG01243.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(22): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(14): Show |
1 | a0002c0005t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.295+1691_295+1692i others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(15): Show |
7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(24): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | C | CTTTTTTT others(16): Show |
1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295+1691_295+1692i others(25): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759246 | CT | C | 13 | a0001c0002t0001g0175 a0001c0002t0001g0233 a0001c0002t0001g0234 others(10): Show |
13 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.295+1691delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | ||||||
| chr4:75759321 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1748C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759321 | |||||||
| chr4:75759736 | C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295+2163C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759736 | |||||||
| chr4:75759883 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.295+2310C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759883 | |||||||
| chr4:75759888 | G | A | 1 | a0001c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.295+2315G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759888 | |||||||
| chr4:75759910 | T | TA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0122 a0001c0002t0001g0283 others(4): Show |
7 | HG01981.hp2 HG02273.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+2354dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759910 | ||||||
| chr4:75759910 | TA | T | 7 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0001g0102 others(4): Show |
7 | HG00639.hp2 HG01109.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+2354delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759910 | ||||||
| chr4:75760073 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295+2500G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760073 | |||||||
| chr4:75760126 | T | C | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+2553T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760126 | |||||||
| chr4:75760219 | A | C | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+2646A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760219 | |||||||
| chr4:75760253 | G | A | 12 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+2680G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760253 | |||||||
| chr4:75760376 | A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295+2803A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760376 | |||||||
| chr4:75760388 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+2815C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760388 | |||||||
| chr4:75760418 | T | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+2845T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760418 | |||||||
| chr4:75760429 | A | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.295+2856A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760429 | |||||||
| chr4:75760872 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.295+3299C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760872 | |||||||
| chr4:75760992 | T | C | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+3419T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760992 | |||||||
| chr4:75761200 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.295+3627T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761200 | |||||||
| chr4:75761202 | A | C | 1 | a0001c0002t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.295+3629A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761202 | |||||||
| chr4:75761326 | T | C | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.295+3753T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761326 | |||||||
| chr4:75761707 | A | C | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+4134A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761707 | |||||||
| chr4:75761734 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.295+4161A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761734 | |||||||
| chr4:75761796 | T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+4223T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761796 | |||||||
| chr4:75762164 | C | CT | 21 | a0001c0001t0001g0040 a0001c0001t0001g0179 a0001c0003t0001g0002 others(18): Show |
22 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.295+4616dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | ||||||
| chr4:75762164 | CT | C | 128 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0047 others(125): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.295+4616delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | ||||||
| chr4:75762164 | CTT | C | 103 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.295+4615_295+4616d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | ||||||
| chr4:75762383 | C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295+4810C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762383 | |||||||
| chr4:75762438 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.295+4865A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762438 | |||||||
| chr4:75762495 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+4922T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762495 | |||||||
| chr4:75762569 | G | T | 1 | a0001c0002t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.295+4996G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762569 | |||||||
| chr4:75762743 | AT | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5171delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762743 | |||||||
| chr4:75762954 | C | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5381C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762954 | |||||||
| chr4:75762955 | A | G | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+5382A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762955 | |||||||
| chr4:75763057 | C | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0138 |
2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.295+5484C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763057 | |||||||
| chr4:75763117 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.295+5544A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763117 | |||||||
| chr4:75763230 | T | C | 3 | a0001c0003t0002g0003 a0001c0003t0002g0004 a0001c0009t0007g0169 |
3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.295+5657T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763230 | |||||||
| chr4:75763419 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.295+5846T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763419 | |||||||
| chr4:75763458 | G | A | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.295+5885G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763458 | |||||||
| chr4:75763480 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5907G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763480 | |||||||
| chr4:75763784 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.295+6211G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763784 | |||||||
| chr4:75764142 | A | G | 5 | a0001c0002t0001g0220 a0002c0005t0001g0218 a0002c0005t0001g0221 others(2): Show |
5 | HG03491.hp1 HG03491.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-6297A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764142 | |||||||
| chr4:75764191 | T | C | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.296-6248T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764191 | |||||||
| chr4:75764442 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0179 |
3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.296-5997A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764442 | |||||||
| chr4:75764523 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.296-5916C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764523 | |||||||
| chr4:75764678 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.296-5761C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764678 | |||||||
| chr4:75764769 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.296-5670T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764769 | |||||||
| chr4:75765040 | A | T | 1 | a0001c0002t0001g0278 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.296-5399A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765040 | |||||||
| chr4:75765143 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.296-5296A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765143 | |||||||
| chr4:75765148 | G | A | 1 | a0001c0006t0001g0215 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.296-5291G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765148 | |||||||
| chr4:75765280 | A | G | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.296-5159A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765280 | |||||||
| chr4:75765316 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.296-5123T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765316 | |||||||
| chr4:75765322 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | NA18962.hp2 NA18966.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-5117A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765322 | |||||||
| chr4:75765384 | A | T | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-5055A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765384 | |||||||
| chr4:75765418 | T | G | 1 | a0001c0002t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.296-5021T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765418 | |||||||
| chr4:75765437 | T | C | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.296-5002T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765437 | |||||||
| chr4:75765447 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.296-4992A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765447 | |||||||
| chr4:75765637 | C | CT | 251 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(248): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.296-4788dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75765637 | ||||||
| chr4:75765653 | C | T | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.296-4786C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765653 | |||||||
| chr4:75765787 | G | C | 144 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(141): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.296-4652G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765787 | |||||||
| chr4:75766038 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-4401C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766038 | |||||||
| chr4:75766139 | A | G | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.296-4300A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766139 | |||||||
| chr4:75766153 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.296-4286T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766153 | |||||||
| chr4:75766391 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.296-4048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766391 | |||||||
| chr4:75766431 | C | T | 2 | a0001c0002t0001g0165 a0001c0002t0001g0282 |
2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.296-4008C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766431 | |||||||
| chr4:75766559 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.296-3880C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766559 | |||||||
| chr4:75766957 | A | G | 2 | a0001c0003t0001g0189 a0001c0003t0001g0203 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.296-3482A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766957 | |||||||
| chr4:75767061 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.296-3378G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767061 | |||||||
| chr4:75767089 | T | C | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.296-3350T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767089 | |||||||
| chr4:75767277 | C | A | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.296-3162C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767277 | |||||||
| chr4:75767735 | T | C | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.296-2704T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767735 | |||||||
| chr4:75767756 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.296-2683G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767756 | |||||||
| chr4:75768390 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-2049A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768390 | |||||||
| chr4:75768450 | T | TA | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.296-1988dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75768450 | ||||||
| chr4:75768517 | A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-1922A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768517 | |||||||
| chr4:75768994 | T | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-1445T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768994 | |||||||
| chr4:75769189 | C | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.296-1250C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769189 | |||||||
| chr4:75769340 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.296-1099C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769340 | |||||||
| chr4:75769392 | G | A | 4 | a0001c0002t0001g0171 a0001c0002t0001g0174 a0001c0002t0001g0175 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-1047G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769392 | |||||||
| chr4:75769599 | G | T | 1 | a0001c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.296-840G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769599 | |||||||
| chr4:75769740 | C | CT | 110 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.296-683dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75769740 | ||||||
| chr4:75769795 | A | C | 1 | a0001c0002t0001g0274 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.296-644A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769795 | |||||||
| chr4:75770095 | C | T | 82 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(79): Show |
82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.296-344C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75770095 | |||||||
| chr4:75770130 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.296-309C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75770130 | |||||||
| chr4:75770553 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.396+14C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770553 | |||||||
| chr4:75770659 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.396+120G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770659 | |||||||
| chr4:75770675 | G | C | 253 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(250): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.396+136G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770675 | |||||||
| chr4:75770697 | CACTT | C | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.397-123_397-120del others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 75770697 | ||||||
| chr4:75771258 | T | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.555+121T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771258 | |||||||
| chr4:75771259 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+122A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771259 | |||||||
| chr4:75771290 | G | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+153G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771290 | |||||||
| chr4:75771302 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.555+165G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771302 | |||||||
| chr4:75771375 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555+238C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771375 | |||||||
| chr4:75771745 | C | T | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.555+608C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771745 | |||||||
| chr4:75771795 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+658G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771795 | |||||||
| chr4:75771813 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0082 others(1): Show |
4 | HG00438.hp2 HG04184.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+676G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771813 | |||||||
| chr4:75771825 | A | G | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+688A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771825 | |||||||
| chr4:75771838 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+701A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771838 | |||||||
| chr4:75771860 | T | C | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+723T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771860 | |||||||
| chr4:75771875 | A | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0179 |
3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.555+738A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771875 | |||||||
| chr4:75772197 | G | A | 13 | a0001c0002t0001g0231 a0001c0002t0001g0236 a0001c0002t0001g0253 others(10): Show |
13 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.555+1060G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772197 | |||||||
| chr4:75772399 | G | A | 137 | a0001c0002t0001g0037 a0001c0002t0001g0152 a0001c0002t0001g0153 others(134): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+1262G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772399 | |||||||
| chr4:75772505 | G | A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.555+1368G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772505 | |||||||
| chr4:75772533 | G | A | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.555+1396G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772533 | |||||||
| chr4:75772674 | T | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.555+1537T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772674 | |||||||
| chr4:75772696 | A | G | 254 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.555+1559A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772696 | |||||||
| chr4:75772751 | AT | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+1617delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75772751 | ||||||
| chr4:75772815 | G | A | 2 | a0001c0002t0001g0255 a0001c0002t0001g0262 |
2 | NA18967.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.555+1678G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772815 | |||||||
| chr4:75772942 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.556-1734C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772942 | |||||||
| chr4:75772949 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.556-1727T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772949 | |||||||
| chr4:75773194 | TTTTA | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | NA18962.hp2 NA19007.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.556-1478_556-1475d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773194 | ||||||
| chr4:75773292 | T | C | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.556-1384T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773292 | |||||||
| chr4:75773312 | A | G | 1 | a0001c0004t0002g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.556-1364A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773312 | |||||||
| chr4:75773365 | TAA | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.556-1308_556-1307d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773365 | ||||||
| chr4:75773389 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.556-1287C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773389 | |||||||
| chr4:75773451 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.556-1225A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773451 | |||||||
| chr4:75773469 | A | G | 72 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(69): Show |
72 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.556-1207A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773469 | |||||||
| chr4:75773502 | A | G | 41 | a0001c0003t0001g0002 a0001c0003t0001g0137 a0001c0003t0001g0154 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-1174A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773502 | |||||||
| chr4:75773638 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.556-1038G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773638 | |||||||
| chr4:75773808 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.556-868T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773808 | |||||||
| chr4:75773913 | CT | C | 255 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(252): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.556-755delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773913 | ||||||
| chr4:75773986 | G | A | 82 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(79): Show |
82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.556-690G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773986 | |||||||
| chr4:75774149 | C | T | 150 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(147): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.556-527C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75774149 | |||||||
| chr4:75774657 | TTCTC | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.556-17_556-14delCT others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75774657 | ||||||
| chr4:75774876 | G | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676+80G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75774876 | |||||||
| chr4:75775079 | T | C | 31 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+283T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775079 | |||||||
| chr4:75775329 | A | G | 2 | a0001c0004t0002g0010 a0001c0004t0002g0031 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.676+533A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775329 | |||||||
| chr4:75775498 | C | T | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+702C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775498 | |||||||
| chr4:75775735 | A | C | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.676+939A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775735 | |||||||
| chr4:75775809 | A | G | 31 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+1013A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775809 | |||||||
| chr4:75775844 | A | G | 5 | a0001c0002t0001g0164 a0001c0002t0001g0167 a0001c0002t0001g0168 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775844 | |||||||
| chr4:75776058 | A | G | 83 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(80): Show |
83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.676+1262A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776058 | |||||||
| chr4:75776101 | A | G | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+1305A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776101 | |||||||
| chr4:75776199 | C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.676+1403C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776199 | |||||||
| chr4:75776230 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.676+1434T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776230 | |||||||
| chr4:75776240 | T | G | 2 | a0001c0003t0001g0189 a0001c0003t0001g0203 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676+1444T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776240 | |||||||
| chr4:75776730 | T | C | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.676+1934T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776730 | |||||||
| chr4:75776770 | A | G | 1 | a0001c0003t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.676+1974A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776770 | |||||||
| chr4:75776811 | G | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676+2015G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776811 | |||||||
| chr4:75776898 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0003g0057 a0001c0001t0003g0072 |
3 | HG02109.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.676+2102A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776898 | |||||||
| chr4:75776918 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.676+2122A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776918 | |||||||
| chr4:75776923 | T | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2127T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776923 | |||||||
| chr4:75776924 | A | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2128A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776924 | |||||||
| chr4:75777171 | A | G | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676+2375A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777171 | |||||||
| chr4:75777271 | A | G | 246 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(243): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.676+2475A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777271 | |||||||
| chr4:75777288 | T | A | 1 | a0001c0002t0001g0231 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.676+2492T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777288 | |||||||
| chr4:75777458 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.676+2662G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777458 | |||||||
| chr4:75777513 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2717A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777513 | |||||||
| chr4:75777715 | C | G | 110 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.676+2919C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777715 | |||||||
| chr4:75777869 | A | G | 8 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0229 others(5): Show |
8 | NA18941.hp2 NA18950.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+3073A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777869 | |||||||
| chr4:75778053 | G | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.676+3257G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778053 | |||||||
| chr4:75778270 | G | T | 1 | a0001c0002t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.676+3474G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778270 | |||||||
| chr4:75778374 | G | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.676+3578G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778374 | |||||||
| chr4:75778463 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+3667A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778463 | |||||||
| chr4:75778469 | G | A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.676+3673G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778469 | |||||||
| chr4:75778502 | C | T | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.676+3706C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778502 | |||||||
| chr4:75778605 | A | G | 2 | a0001c0006t0001g0215 a0001c0006t0001g0216 |
2 | HG01516.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.676+3809A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778605 | |||||||
| chr4:75778737 | A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676+3941A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778737 | |||||||
| chr4:75778786 | G | A | 73 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(70): Show |
73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.677-3894G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778786 | |||||||
| chr4:75778841 | A | G | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.677-3839A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778841 | |||||||
| chr4:75778981 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.677-3699C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778981 | |||||||
| chr4:75779382 | G | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-3298G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779382 | |||||||
| chr4:75779562 | A | G | 1 | a0001c0002t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.677-3118A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779562 | |||||||
| chr4:75779630 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-3050A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779630 | |||||||
| chr4:75779714 | A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2966A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779714 | |||||||
| chr4:75779750 | A | G | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.677-2930A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779750 | |||||||
| chr4:75779942 | G | A | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.677-2738G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779942 | |||||||
| chr4:75779948 | A | G | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.677-2732A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779948 | |||||||
| chr4:75779994 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.677-2686A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779994 | |||||||
| chr4:75780335 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.677-2345C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75780335 | |||||||
| chr4:75780567 | A | AGCCAATA others(2282): Show |
1 | a0001c0004t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.677-2095_677-2094i others(2291): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780567 | ||||||
| chr4:75780640 | C | CT | 69 | a0001c0001t0001g0039 a0001c0002t0001g0037 a0001c0002t0001g0153 others(66): Show |
69 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(66): Show |
intron_variant | MODIFIER | c.677-2015dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780640 | C | CTT | 25 | a0001c0002t0001g0156 a0001c0002t0001g0160 a0001c0002t0001g0164 others(22): Show |
25 | HG00609.hp2 HG01346.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.677-2016_677-2015d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780640 | C | CTTTT | 23 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(20): Show |
24 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-2018_677-2015d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780640 | C | CTTTTT | 6 | a0001c0004t0002g0017 a0001c0004t0002g0025 a0001c0004t0002g0029 others(3): Show |
6 | HG01109.hp2 HG01346.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-2019_677-2015d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780640 | C | CTTTTTTT others(4): Show |
1 | a0001c0004t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.677-2025_677-2015d others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780640 | CT | C | 93 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.677-2015delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | ||||||
| chr4:75780792 | T | C | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.677-1888T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75780792 | |||||||
| chr4:75781156 | A | C | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-1524A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781156 | |||||||
| chr4:75781340 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.677-1340G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781340 | |||||||
| chr4:75781529 | T | A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.677-1151T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781529 | |||||||
| chr4:75781760 | TA | T | 111 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.677-910delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75781760 | ||||||
| chr4:75781761 | A | T | 1 | a0001c0003t0001g0202 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.677-919A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781761 | |||||||
| chr4:75781904 | T | G | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.677-776T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781904 | |||||||
| chr4:75782353 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.677-327A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75782353 | |||||||
| chr4:75783325 | C | T | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.855+467C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783325 | |||||||
| chr4:75783526 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.855+668A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783526 | |||||||
| chr4:75783613 | C | T | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.855+755C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783613 | |||||||
| chr4:75783626 | C | A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.855+768C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783626 | |||||||
| chr4:75783674 | C | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.855+816C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783674 | |||||||
| chr4:75783707 | A | G | 108 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.855+849A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783707 | |||||||
| chr4:75783714 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.855+856G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783714 | |||||||
| chr4:75783861 | A | T | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.855+1003A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783861 | |||||||
| chr4:75784132 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.855+1274C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784132 | |||||||
| chr4:75784626 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.855+1768A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784626 | |||||||
| chr4:75784791 | G | GA | 8 | a0001c0001t0001g0139 a0001c0004t0001g0049 a0001c0004t0002g0018 others(5): Show |
8 | HG01993.hp2 NA18970.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.855+1947dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr4 | 75784791 | ||||||
| chr4:75784940 | T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.855+2082T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784940 | |||||||
| chr4:75785174 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.856-1888A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785174 | |||||||
| chr4:75785204 | G | A | 2 | a0001c0002t0001g0230 a0001c0002t0001g0284 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.856-1858G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785204 | |||||||
| chr4:75785323 | T | C | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.856-1739T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785323 | |||||||
| chr4:75785362 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0097 a0001c0001t0001g0107 others(5): Show |
8 | HG01891.hp1 HG02922.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-1700T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785362 | |||||||
| chr4:75785413 | C | G | 1 | a0001c0003t0001g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.856-1649C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785413 | |||||||
| chr4:75785543 | C | T | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.856-1519C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785543 | |||||||
| chr4:75785548 | A | G | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-1514A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785548 | |||||||
| chr4:75785704 | A | G | 1 | a0001c0004t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856-1358A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785704 | |||||||
| chr4:75785741 | A | G | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.856-1321A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785741 | |||||||
| chr4:75785755 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.856-1307A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785755 | |||||||
| chr4:75785927 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1135A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785927 | |||||||
| chr4:75786456 | CTG | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.856-602_856-601del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr4 | 75786456 | ||||||
| chr4:75786775 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856-287G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786775 | |||||||
| chr4:75786793 | T | C | 10 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0267 others(7): Show |
10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-269T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786793 | |||||||
| chr4:75786897 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-165A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786897 | |||||||
| chr4:75786924 | C | T | 4 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0099 others(1): Show |
4 | HG00639.hp1 HG00738.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-138C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786924 | |||||||
| chr4:75787349 | A | G | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.996+147A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787349 | |||||||
| chr4:75787403 | T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.996+201T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787403 | |||||||
| chr4:75787479 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.996+277G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787479 | |||||||
| chr4:75787539 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.996+337C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787539 | |||||||
| chr4:75787702 | T | C | 1 | a0001c0004t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.996+500T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787702 | |||||||
| chr4:75787737 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.996+535C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787737 | |||||||
| chr4:75788145 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0102 others(2): Show |
5 | HG01975.hp1 HG02004.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+943C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788145 | |||||||
| chr4:75788165 | TTA | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+965_996+966del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788165 | ||||||
| chr4:75788166 | TA | T | 4 | a0001c0001t0001g0118 a0001c0003t0002g0003 a0001c0003t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.996+965delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788166 | |||||||
| chr4:75788167 | A | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.996+965A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788167 | |||||||
| chr4:75788170 | T | A | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.996+968T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788170 | |||||||
| chr4:75788170 | TA | T | 47 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0117 others(44): Show |
47 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.996+969delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788170 | |||||||
| chr4:75788171 | A | T | 18 | a0001c0001t0001g0118 a0001c0001t0001g0134 a0001c0002t0001g0167 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.996+969A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788171 | |||||||
| chr4:75788171 | AT | A | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.996+984delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788171 | ||||||
| chr4:75788172 | T | A | 1 | a0001c0003t0001g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.996+970T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788172 | |||||||
| chr4:75788172 | T | TTTA | 30 | a0001c0001t0001g0112 a0001c0004t0001g0049 a0001c0004t0002g0001 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.996+972_996+973ins others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788172 | ||||||
| chr4:75788175 | T | A | 23 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0267 others(20): Show |
23 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.996+973T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788175 | |||||||
| chr4:75788176 | T | A | 43 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0045 others(40): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.996+974T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788176 | |||||||
| chr4:75788180 | T | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.996+978T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788180 | |||||||
| chr4:75788266 | C | T | 1 | a0001c0002t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.996+1064C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788266 | |||||||
| chr4:75788329 | G | A | 2 | a0001c0004t0002g0001 a0001c0004t0002g0034 |
3 | HG00099.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.996+1127G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788329 | |||||||
| chr4:75788382 | G | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.996+1180G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788382 | |||||||
| chr4:75788478 | A | C | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.996+1276A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788478 | |||||||
| chr4:75788547 | C | CTT | 35 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(32): Show |
36 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.996+1356_996+1357d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788547 | ||||||
| chr4:75788659 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0120 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.996+1457C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788659 | |||||||
| chr4:75788764 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.997-1386C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788764 | |||||||
| chr4:75788826 | C | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.997-1324C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788826 | |||||||
| chr4:75789096 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.997-1054G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789096 | |||||||
| chr4:75789230 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997-920T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789230 | |||||||
| chr4:75789282 | C | CTGT | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.997-857_997-855dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75789282 | ||||||
| chr4:75789317 | T | C | 6 | a0001c0003t0001g0185 a0001c0003t0001g0209 a0001c0003t0001g0210 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.997-833T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789317 | |||||||
| chr4:75789334 | G | A | 2 | a0001c0003t0001g0194 a0001c0003t0001g0195 |
2 | HG00741.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.997-816G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789334 | |||||||
| chr4:75789474 | C | T | 2 | a0001c0007t0001g0101 a0001c0007t0001g0151 |
2 | HG01123.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.997-676C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789474 | |||||||
| chr4:75789498 | C | T | 10 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0267 others(7): Show |
10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-652C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789498 | |||||||
| chr4:75789731 | A | G | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.997-419A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789731 | |||||||
| chr4:75789925 | T | C | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.997-225T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789925 | |||||||
| chr4:75789937 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-213T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789937 | |||||||
| chr4:75789938 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-212T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789938 | |||||||
| chr4:75789944 | T | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.997-206T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789944 | |||||||
| chr4:75789964 | G | A | 5 | a0001c0003t0001g0181 a0001c0003t0001g0188 a0001c0003t0001g0192 others(2): Show |
5 | HG01123.hp1 HG01934.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-186G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789964 | |||||||
| chr4:75790047 | T | TA | 84 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(81): Show |
84 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.997-92dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790047 | ||||||
| chr4:75790047 | TA | T | 132 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.997-92delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790047 | ||||||
| chr4:75790049 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0132 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.997-101A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790049 | |||||||
| chr4:75790058 | A | AAC | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-92_997-91insAC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790058 | |||||||
| chr4:75790059 | C | A | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-91C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790059 | |||||||
| chr4:75790069 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-81A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790069 | |||||||
| chr4:75790070 | G | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0098 a0001c0001t0001g0104 others(2): Show |
5 | HG00280.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-80G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790070 | |||||||
| chr4:75790071 | AT | A | 30 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.997-71delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790071 | ||||||
| chr4:75790073 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.997-77T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790073 | |||||||
| chr4:75790911 | G | GA | 41 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+126dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75790911 | ||||||
| chr4:75791020 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1240+223A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791020 | |||||||
| chr4:75791265 | C | T | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1240+468C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791265 | |||||||
| chr4:75791309 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1240+512A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791309 | |||||||
| chr4:75791422 | G | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1240+625G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791422 | |||||||
| chr4:75791517 | G | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1240+720G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791517 | |||||||
| chr4:75791617 | C | G | 1 | a0001c0006t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1240+820C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791617 | |||||||
| chr4:75791800 | CA | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1240+1012delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75791800 | ||||||
| chr4:75791810 | T | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1240+1013T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791810 | |||||||
| chr4:75791970 | G | A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.1240+1173G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791970 | |||||||
| chr4:75791985 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1240+1188C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791985 | |||||||
| chr4:75792022 | C | CT | 32 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(29): Show |
32 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1240+1241dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75792022 | ||||||
| chr4:75792022 | CT | C | 7 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0002t0001g0153 others(4): Show |
7 | HG01169.hp2 HG01943.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+1241delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75792022 | ||||||
| chr4:75792426 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1241-1264A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75792426 | |||||||
| chr4:75792618 | G | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1241-1072G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75792618 | |||||||
| chr4:75793205 | CT | C | 80 | a0001c0001t0001g0048 a0001c0001t0001g0117 a0001c0002t0001g0037 others(77): Show |
80 | HG00609.hp2 HG01109.hp1 HG01169.hp2 others(77): Show |
intron_variant | MODIFIER | c.1241-462delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | ||||||
| chr4:75793205 | CTT | C | 113 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(110): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1241-463_1241-462d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | ||||||
| chr4:75793205 | CTTT | C | 30 | a0001c0001t0001g0040 a0001c0001t0001g0122 a0001c0001t0001g0139 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1241-464_1241-462d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | ||||||
| chr4:75793368 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1241-322C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75793368 | |||||||
| chr4:75793623 | A | G | 1 | a0001c0003t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1241-67A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75793623 | |||||||
| chr4:75794056 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1452+155G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794056 | |||||||
| chr4:75794152 | T | G | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+251T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794152 | |||||||
| chr4:75794200 | C | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1452+299C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794200 | |||||||
| chr4:75794355 | C | T | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+454C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794355 | |||||||
| chr4:75794479 | T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1452+578T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794479 | |||||||
| chr4:75794525 | T | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1452+624T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794525 | |||||||
| chr4:75794608 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1452+707G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794608 | |||||||
| chr4:75794678 | T | C | 1 | a0001c0003t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1452+777T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794678 | |||||||
| chr4:75794894 | T | C | 2 | a0001c0004t0002g0024 a0001c0014t0002g0036 |
2 | HG03453.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1452+993T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794894 | |||||||
| chr4:75795209 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1452+1308A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795209 | |||||||
| chr4:75795354 | C | T | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+1453C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795354 | |||||||
| chr4:75795562 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1452+1661G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795562 | |||||||
| chr4:75795646 | G | A | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1452+1745G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795646 | |||||||
| chr4:75795708 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1452+1807G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795708 | |||||||
| chr4:75795769 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1452+1868C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795769 | |||||||
| chr4:75795914 | TTTTTG | T | 238 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(235): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1452+2045_1452+204 others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75795914 | ||||||
| chr4:75796140 | A | G | 1 | a0001c0002t0001g0265 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1452+2239A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796140 | |||||||
| chr4:75796318 | ATCCCAGA others(4): Show |
A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1452+2421_1452+243 others(15): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796318 | ||||||
| chr4:75796341 | C | CTTTTTTT others(7): Show |
3 | a0001c0004t0002g0019 a0001c0004t0002g0026 a0001c0014t0002g0036 |
3 | HG03453.hp2 HG03704.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(18): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(8): Show |
25 | a0001c0001t0001g0041 a0001c0004t0001g0049 a0001c0004t0002g0001 others(22): Show |
26 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(19): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | HG00140.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(20): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(10): Show |
91 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(11): Show |
15 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0061 others(12): Show |
15 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(22): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0118 |
2 | HG04115.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796341 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1452+2452_1452+245 others(25): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | ||||||
| chr4:75796351 | T | TTTTTTTT others(10): Show |
1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1452+2452_1452+245 others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796351 | ||||||
| chr4:75796493 | A | G | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1452+2592A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796493 | |||||||
| chr4:75796500 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1452+2599G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796500 | |||||||
| chr4:75796571 | G | T | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1452+2670G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796571 | |||||||
| chr4:75796829 | A | G | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1453-2793A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796829 | |||||||
| chr4:75796842 | A | G | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1453-2780A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796842 | |||||||
| chr4:75796875 | AT | A | 112 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1453-2732delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796875 | ||||||
| chr4:75796875 | ATT | A | 30 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1453-2733_1453-273 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796875 | ||||||
| chr4:75796890 | T | TC | 16 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(13): Show |
16 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1453-2731dupC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796890 | ||||||
| chr4:75796953 | T | C | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.1453-2669T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796953 | |||||||
| chr4:75797171 | A | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1453-2451A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797171 | |||||||
| chr4:75797178 | C | A | 1 | a0001c0002t0001g0278 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1453-2444C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797178 | |||||||
| chr4:75797221 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1453-2401T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797221 | |||||||
| chr4:75797474 | C | CTT | 120 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(117): Show |
121 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1453-2147_1453-214 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797474 | ||||||
| chr4:75797474 | CTCTTT | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1453-2146_1453-214 others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797474 | ||||||
| chr4:75797560 | C | CA | 106 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1453-2046dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797560 | ||||||
| chr4:75797560 | CA | C | 87 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(84): Show |
87 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.1453-2046delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797560 | ||||||
| chr4:75797686 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1453-1936G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797686 | |||||||
| chr4:75797726 | C | G | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-1896C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797726 | |||||||
| chr4:75797790 | C | T | 29 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1453-1832C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797790 | |||||||
| chr4:75797947 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0143 |
2 | HG01175.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1453-1675G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797947 | |||||||
| chr4:75797966 | G | A | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1453-1656G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797966 | |||||||
| chr4:75798231 | C | T | 240 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(237): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1453-1391C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798231 | |||||||
| chr4:75798248 | C | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1374C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798248 | |||||||
| chr4:75798259 | C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1363C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798259 | |||||||
| chr4:75798297 | G | A | 10 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0267 others(7): Show |
10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-1325G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798297 | |||||||
| chr4:75798387 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1453-1235G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798387 | |||||||
| chr4:75798395 | G | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1453-1227G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798395 | |||||||
| chr4:75798574 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1453-1048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798574 | |||||||
| chr4:75798600 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1022T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798600 | |||||||
| chr4:75798703 | G | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-919G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798703 | |||||||
| chr4:75798821 | A | AGTTTT | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1453-790_1453-786d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75798821 | ||||||
| chr4:75799148 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-474G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799148 | |||||||
| chr4:75799189 | G | GT | 37 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1453-433_1453-432i others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799189 | |||||||
| chr4:75799206 | G | A | 5 | a0001c0002t0001g0164 a0001c0002t0001g0167 a0001c0002t0001g0168 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1453-416G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799206 | |||||||
| chr4:75799259 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1453-363A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799259 | |||||||
| chr4:75799319 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0098 |
2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1453-303C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799319 | |||||||
| chr4:75799374 | A | G | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1453-248A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799374 | |||||||
| chr4:75799610 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1453-12T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799610 | |||||||
| chr4:75799614 | T | C | 3 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0212 |
3 | HG02258.hp1 HG02630.hp2 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.1453-8T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799614 | |||||||
| chr4:75799822 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563+90A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799822 | |||||||
| chr4:75799897 | G | C | 83 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(80): Show |
83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.1563+165G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799897 | |||||||
| chr4:75799920 | C | G | 2 | a0001c0004t0002g0019 a0001c0004t0002g0020 |
2 | NA18980.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1563+188C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799920 | |||||||
| chr4:75799922 | G | A | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563+190G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799922 | |||||||
| chr4:75800012 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1563+280C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800012 | |||||||
| chr4:75800167 | C | T | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1564-184C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800167 | |||||||
| chr4:75800261 | C | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1564-90C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800261 | |||||||
| chr4:75800306 | G | A | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1564-45G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800306 | |||||||
| chr4:75800518 | C | CTTT | 103 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(100): Show |
103 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1682+62_1682+64dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | ||||||
| chr4:75800518 | C | CTTTT | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(8): Show |
11 | HG01123.hp2 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1682+61_1682+64dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | ||||||
| chr4:75800518 | CT | C | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1682+64delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | ||||||
| chr4:75800552 | C | G | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1683-66C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | chr4 | 75800552 | |||||||
| chr4:75800602 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0179 |
3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1683-16A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | chr4 | 75800602 | |||||||
| chr4:75800888 | G | A | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1864+89G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 16/23 | chr4 | 75800888 | |||||||
| chr4:75801269 | T | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1986+69T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801269 | |||||||
| chr4:75801397 | A | G | 1 | a0001c0004t0002g0031 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1986+197A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801397 | |||||||
| chr4:75801426 | C | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1986+226C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801426 | |||||||
| chr4:75801502 | C | G | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1986+302C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801502 | |||||||
| chr4:75801683 | C | T | 1 | a0001c0002t0001g0272 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1986+483C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801683 | |||||||
| chr4:75801747 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1986+547A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801747 | |||||||
| chr4:75801943 | G | A | 3 | a0001c0003t0001g0154 a0001c0003t0001g0196 a0001c0003t0001g0202 |
3 | HG01192.hp1 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1986+743G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801943 | |||||||
| chr4:75801977 | G | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1986+777G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801977 | |||||||
| chr4:75802184 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1986+984G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802184 | |||||||
| chr4:75802584 | C | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1986+1384C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802584 | |||||||
| chr4:75802585 | A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1986+1385A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802585 | |||||||
| chr4:75802736 | C | CT | 44 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0092 others(41): Show |
44 | HG00609.hp2 HG01243.hp2 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.1987-1373dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | ||||||
| chr4:75802736 | C | CTT | 9 | a0001c0001t0001g0039 a0001c0002t0001g0156 a0001c0002t0001g0165 others(6): Show |
9 | HG01109.hp1 HG02145.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1987-1374_1987-137 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | ||||||
| chr4:75802736 | CT | C | 78 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1987-1373delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | ||||||
| chr4:75802736 | CTT | C | 30 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0004t0002g0001 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1987-1374_1987-137 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | ||||||
| chr4:75802742 | T | C | 2 | a0001c0001t0001g0139 a0006c0016t0001g0180 |
2 | HG01993.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1987-1392T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802742 | |||||||
| chr4:75802764 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0140 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1987-1370G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802764 | |||||||
| chr4:75802777 | T | C | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1987-1357T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802777 | |||||||
| chr4:75802791 | G | A | 29 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1987-1343G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802791 | |||||||
| chr4:75802872 | C | T | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1987-1262C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802872 | |||||||
| chr4:75802880 | C | T | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1987-1254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802880 | |||||||
| chr4:75802887 | A | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1987-1247A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802887 | |||||||
| chr4:75803087 | C | CA | 110 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1987-1034dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75803087 | ||||||
| chr4:75803087 | C | CAA | 11 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0056 others(8): Show |
11 | HG00738.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1987-1035_1987-103 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75803087 | ||||||
| chr4:75803100 | A | C | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1987-1034A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803100 | |||||||
| chr4:75803238 | G | C | 5 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0070 others(2): Show |
5 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1987-896G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803238 | |||||||
| chr4:75803284 | A | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1987-850A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803284 | |||||||
| chr4:75803365 | T | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1987-769T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803365 | |||||||
| chr4:75803522 | C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1987-612C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803522 | |||||||
| chr4:75803527 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1987-607G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803527 | |||||||
| chr4:75803762 | T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-372T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803762 | |||||||
| chr4:75803795 | C | T | 2 | a0001c0002t0001g0230 a0001c0002t0001g0284 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1987-339C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803795 | |||||||
| chr4:75803834 | T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-300T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803834 | |||||||
| chr4:75803856 | A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-278A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803856 | |||||||
| chr4:75803924 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1987-210C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803924 | |||||||
| chr4:75803940 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1987-194G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803940 | |||||||
| chr4:75804075 | A | G | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1987-59A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75804075 | |||||||
| chr4:75804092 | G | T | 273 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1987-42G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75804092 | |||||||
| chr4:75804393 | A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2125+121A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804393 | |||||||
| chr4:75804454 | T | C | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2125+182T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804454 | |||||||
| chr4:75804471 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2125+199A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804471 | |||||||
| chr4:75804817 | G | A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.2126-323G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804817 | |||||||
| chr4:75804911 | C | G | 30 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2126-229C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804911 | |||||||
| chr4:75804921 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2126-219C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804921 | |||||||
| chr4:75804967 | A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2126-173A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804967 | |||||||
| chr4:75805026 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2126-114A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805026 | |||||||
| chr4:75805065 | A | G | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2126-75A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805065 | |||||||
| chr4:75805106 | C | T | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-34C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805106 | |||||||
| chr4:75805127 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2126-13G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805127 | |||||||
| chr4:75805363 | C | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2289+60C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805363 | |||||||
| chr4:75805375 | T | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2289+72T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805375 | |||||||
| chr4:75805386 | C | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2289+83C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805386 | |||||||
| chr4:75805468 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2289+165A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805468 | |||||||
| chr4:75805685 | T | C | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2289+382T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805685 | |||||||
| chr4:75805709 | TA | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0102 a0001c0001t0001g0122 others(3): Show |
6 | HG01517.hp1 HG01975.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.2289+423delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 75805709 | ||||||
| chr4:75805770 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2289+467A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805770 | |||||||
| chr4:75805797 | A | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0179 |
3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2289+494A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805797 | |||||||
| chr4:75805932 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2290-554T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805932 | |||||||
| chr4:75805944 | C | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-542C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805944 | |||||||
| chr4:75805945 | G | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-541G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805945 | |||||||
| chr4:75806128 | A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-358A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806128 | |||||||
| chr4:75806129 | T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-357T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806129 | |||||||
| chr4:75806192 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2290-294G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806192 | |||||||
| chr4:75806304 | A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-182A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806304 | |||||||
| chr4:75806423 | GT | G | 115 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(112): Show |
115 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2290-54delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 75806423 | ||||||
| chr4:75806779 | C | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2376+207C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75806779 | |||||||
| chr4:75806974 | A | G | 51 | a0001c0002t0001g0219 a0001c0002t0001g0220 a0001c0002t0001g0223 others(48): Show |
51 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.2376+402A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75806974 | |||||||
| chr4:75807306 | T | C | 29 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.2376+734T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807306 | |||||||
| chr4:75807502 | C | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2376+930C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807502 | |||||||
| chr4:75807559 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2376+987T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807559 | |||||||
| chr4:75807668 | CTT | C | 31 | a0001c0004t0001g0049 a0001c0004t0002g0001 a0001c0004t0002g0007 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.2376+1099_2376+110 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75807668 | ||||||
| chr4:75807774 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2377-1179A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807774 | |||||||
| chr4:75808038 | A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-915A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808038 | |||||||
| chr4:75808039 | G | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-914G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808039 | |||||||
| chr4:75808103 | T | C | 51 | a0001c0002t0001g0219 a0001c0002t0001g0220 a0001c0002t0001g0223 others(48): Show |
51 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.2377-850T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808103 | |||||||
| chr4:75808107 | C | T | 2 | a0001c0003t0002g0003 a0001c0003t0002g0004 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2377-846C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808107 | |||||||
| chr4:75808473 | T | A | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2377-480T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808473 | |||||||
| chr4:75808621 | A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-332A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808621 | |||||||
| chr4:75808631 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2377-322A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808631 | |||||||
| chr4:75808739 | A | ATT | 39 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0118 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2377-203_2377-202d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75808739 | ||||||
| chr4:75808739 | A | ATTT | 107 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2377-204_2377-202d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75808739 | ||||||
| chr4:75808768 | G | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-185G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808768 | |||||||
| chr4:75808771 | A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-182A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808771 | |||||||
| chr4:75808779 | T | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-174T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808779 | |||||||
| chr4:75808780 | A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-173A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808780 | |||||||
| chr4:75808784 | G | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0068 others(13): Show |
16 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2377-169G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808784 | |||||||
| chr4:75808851 | G | C | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2377-102G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808851 | |||||||
| chr4:75808908 | T | A | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2377-45T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808908 | |||||||
| chr4:75809105 | T | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+54T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809105 | |||||||
| chr4:75809156 | CTTTAGAT others(14): Show |
C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+107_2475+127d others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 75809156 | ||||||
| chr4:75809220 | T | C | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+169T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809220 | |||||||
| chr4:75809233 | C | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.2475+182C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809233 | |||||||
| chr4:75809282 | C | T | 1 | a0001c0004t0002g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2475+231C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809282 | |||||||
| chr4:75809291 | T | A | 91 | a0001c0002t0001g0037 a0001c0002t0001g0155 a0001c0002t0001g0156 others(88): Show |
91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.2475+240T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809291 | |||||||
| chr4:75809309 | G | GA | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+258_2475+259i others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809309 | |||||||
| chr4:75809310 | C | T | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+259C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809310 | |||||||
| chr4:75809348 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2475+297G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809348 | |||||||
| chr4:75809404 | G | T | 1 | a0001c0002t0001g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2475+353G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809404 | |||||||
| chr4:75809532 | G | A | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2475+481G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809532 | |||||||
| chr4:75809599 | A | G | 1 | a0001c0003t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2475+548A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809599 | |||||||
| chr4:75809647 | G | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2475+596G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809647 | |||||||
| chr4:75809755 | T | C | 238 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(235): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2476-677T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809755 | |||||||
| chr4:75810094 | A | T | 2 | a0001c0002t0001g0275 a0001c0002t0001g0276 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2476-338A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810094 | |||||||
| chr4:75810177 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2476-255C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810177 | |||||||
| chr4:75810179 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2476-253T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810179 | |||||||
| chr4:75810275 | G | C | 1 | a0001c0004t0002g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2476-157G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810275 | |||||||
| chr4:75810587 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2583+48A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810587 | |||||||
| chr4:75810604 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0132 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2583+65A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810604 | |||||||
| chr4:75810668 | T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2583+129T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810668 | |||||||
| chr4:75810965 | G | A | 1 | a0001c0003t0001g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2583+426G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810965 | |||||||
| chr4:75810990 | A | G | 1 | a0008c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2583+451A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810990 | |||||||
| chr4:75811143 | C | T | 4 | a0001c0002t0001g0171 a0001c0002t0001g0174 a0001c0002t0001g0175 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583+604C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811143 | |||||||
| chr4:75811157 | C | T | 4 | a0001c0002t0001g0171 a0001c0002t0001g0174 a0001c0002t0001g0175 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583+618C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811157 | |||||||
| chr4:75811217 | A | T | 2 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2583+678A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811217 | |||||||
| chr4:75811243 | C | T | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2583+704C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811243 | |||||||
| chr4:75811312 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2583+773T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811312 | |||||||
| chr4:75811323 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2583+784T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811323 | |||||||
| chr4:75811409 | G | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2584-751G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811409 | |||||||
| chr4:75811416 | C | A | 7 | a0001c0002t0001g0225 a0001c0002t0001g0237 a0001c0002t0001g0242 others(4): Show |
7 | HG00609.hp2 NA18940.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2584-744C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811416 | |||||||
| chr4:75811416 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2584-744C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811416 | |||||||
| chr4:75811417 | C | G | 1 | a0007c0015t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2584-743C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811417 | |||||||
| chr4:75811460 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2584-700T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811460 | |||||||
| chr4:75811555 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2584-605G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811555 | |||||||
| chr4:75811577 | C | G | 38 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.2584-583C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811577 | |||||||
| chr4:75811828 | C | G | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2584-332C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811828 | |||||||
| chr4:75811916 | G | A | 1 | a0006c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2584-244G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811916 | |||||||
| chr4:75812426 | G | T | 1 | a0001c0002t0001g0248 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2799+51G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812426 | |||||||
| chr4:75812579 | C | T | 147 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2799+204C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812579 | |||||||
| chr4:75812701 | G | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2799+326G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812701 | |||||||
| chr4:75812967 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2800-239A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812967 | |||||||
| chr4:75813010 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800-196G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813010 | |||||||
| chr4:75813023 | T | G | 148 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(145): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2800-183T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813023 | |||||||
| chr4:75813067 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2800-139C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813067 | |||||||
| chr4:75813090 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2800-116G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813090 | |||||||
| chr4:75813190 | C | T | 83 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2800-16C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813190 |