Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 641700 |
| ensemblid | ENSG00000249751.4 |
| hgncid | 35454 |
| symbol | ECSCR |
| name | endothelial cell surface expressed chemotaxis and apoptosis regulator |
| refseq_nuc | NM_001077693.4 |
| refseq_prot | NP_001071161.1 |
| ensembl_nuc | ENST00000618155.3 |
| ensembl_prot | ENSP00000479243.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 139448560 |
| end | 139462743 |
| strand | - |
| ver | v1.2 |
| region | chr5:139448560-139462743 |
| region5000 | chr5:139443560-139467743 |
| regionname0 | ECSCR_chr5_139448560_139462743 |
| regionname5000 | ECSCR_chr5_139443560_139467743 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 205 | 368 | 84 | 70 | 163 | 16 | 34 | 123 | ECSCR_chr5_139443560_139467743 | ECSCR | MGTAG others(200): Show |
chr5 | 139443560 | 139467743 |
| a0002 | 0/0 | 205 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | MGTAG others(200): Show |
chr5 | 139443560 | 139467743 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 615 | 368 | 84 | 70 | 163 | 16 | 34 | ECSCR_chr5_139443560_139467743 | ECSCR | ATGGG others(610): Show |
chr5 | 139443560 | 139467743 | ||
| a0002c0002 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | ATGGG others(610): Show |
chr5 | 139443560 | 139467743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1031 | 367 | 84 | 70 | 163 | 16 | 33 | ECSCR_chr5_139443560_139467743 | ECSCR | ACTCC others(1026): Show |
chr5 | 139443560 | 139467743 |
| a0001c0001t0002 | 0/0 | 1031 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | ACTCC others(1026): Show |
chr5 | 139443560 | 139467743 |
| a0002c0002t0001 | 0/0 | 1031 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | ACTCC others(1026): Show |
chr5 | 139443560 | 139467743 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 57 | 3 | 14 | 33 | 5 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0002 | 0/0 | 51 | 9 | 6 | 29 | 4 | 3 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 2 | 13 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0004 | 0/0 | 15 | 1 | 6 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0084 | REF | REF | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139449093 | A | T | 1 | a0002 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.594T>A | p.Ser198Arg | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 9/10 | 667/1031 | 594/618 | 198/205 | chr5 | 139449093 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139448634 | G | C | 1 | a0001c0001t0002 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 10/10 | 266 | chr5 | 139448634 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139448957 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(16): Show |
30 | HG01243.hp2 HG02129.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.610-49T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 9/9 | chr5 | 139448957 | |||||||
| chr5:139449297 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-123A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449297 | |||||||
| chr5:139449351 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513-177T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449351 | |||||||
| chr5:139449430 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0150 |
3 | HG01081.hp1 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.513-256G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449430 | |||||||
| chr5:139449441 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.513-267C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449441 | |||||||
| chr5:139449459 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513-285A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449459 | |||||||
| chr5:139449703 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-529G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449703 | |||||||
| chr5:139449876 | C | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.513-702G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449876 | |||||||
| chr5:139449895 | AT | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0080 others(2): Show |
6 | HG01517.hp2 HG02015.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-722delA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449895 | |||||||
| chr5:139449907 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.513-733A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449907 | |||||||
| chr5:139450033 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.513-859A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450033 | |||||||
| chr5:139450236 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.513-1062G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450236 | |||||||
| chr5:139450335 | T | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513-1161A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450335 | |||||||
| chr5:139450337 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.513-1163A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450337 | |||||||
| chr5:139450434 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0156 |
3 | HG00639.hp2 HG00733.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.513-1260C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450434 | |||||||
| chr5:139450464 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.513-1290C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450464 | |||||||
| chr5:139450478 | T | TA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0089 others(2): Show |
8 | HG01261.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-1305dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | |||||||
| chr5:139450478 | TA | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0001c0001t0001g0093 others(3): Show |
7 | HG00408.hp1 HG01192.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-1305delT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | |||||||
| chr5:139450478 | TAA | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.513-1306_513-1305d others(4): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | |||||||
| chr5:139450551 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.513-1377C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450551 | |||||||
| chr5:139450669 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.513-1495C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450669 | |||||||
| chr5:139450740 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.513-1566G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450740 | |||||||
| chr5:139450906 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.513-1732C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450906 | |||||||
| chr5:139451009 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0102 |
2 | HG00621.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.513-1835C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451009 | |||||||
| chr5:139451111 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0112 |
3 | NA18985.hp2 NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.513-1937C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451111 | |||||||
| chr5:139451354 | T | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.513-2180A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451354 | |||||||
| chr5:139451368 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513-2194C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451368 | |||||||
| chr5:139451430 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0062 a0001c0001t0001g0124 |
5 | HG02622.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-2256A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451430 | |||||||
| chr5:139451488 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-2314C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451488 | |||||||
| chr5:139451744 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0024 others(7): Show |
18 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.513-2570C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451744 | |||||||
| chr5:139451901 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.512+2701A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451901 | |||||||
| chr5:139451941 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+2661A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451941 | |||||||
| chr5:139451943 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0085 |
2 | HG03490.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.512+2659T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451943 | |||||||
| chr5:139452163 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.512+2439A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452163 | |||||||
| chr5:139452226 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.512+2376C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452226 | |||||||
| chr5:139452272 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.512+2330A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452272 | |||||||
| chr5:139452335 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.512+2267C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452335 | |||||||
| chr5:139452659 | GNNNNNNN others(690): Show |
G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1246_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | |||||||
| chr5:139452659 | GNNNNNNN others(730): Show |
G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1206_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | |||||||
| chr5:139452659 | GNNNNNNN others(738): Show |
G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1198_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | |||||||
| chr5:139452660 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1942G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452660 | |||||||
| chr5:139452661 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1941T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452661 | |||||||
| chr5:139452662 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1940T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452662 | |||||||
| chr5:139452663 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1939T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452663 | |||||||
| chr5:139452664 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1938T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452664 | |||||||
| chr5:139452665 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1937T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452665 | |||||||
| chr5:139452666 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1936T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452666 | |||||||
| chr5:139452667 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1935T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452667 | |||||||
| chr5:139452668 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1934T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452668 | |||||||
| chr5:139452669 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1933T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452669 | |||||||
| chr5:139452670 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1932T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452670 | |||||||
| chr5:139452671 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1931G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452671 | |||||||
| chr5:139452672 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1930T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452672 | |||||||
| chr5:139452673 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1929T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452673 | |||||||
| chr5:139452674 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1928T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452674 | |||||||
| chr5:139452675 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1927T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452675 | |||||||
| chr5:139452676 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1926T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452676 | |||||||
| chr5:139452677 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1925T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452677 | |||||||
| chr5:139452678 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1924T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452678 | |||||||
| chr5:139452679 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1923G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452679 | |||||||
| chr5:139452680 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1922T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452680 | |||||||
| chr5:139452681 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1921T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452681 | |||||||
| chr5:139452682 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1920T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452682 | |||||||
| chr5:139452683 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1919T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452683 | |||||||
| chr5:139452684 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1918T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452684 | |||||||
| chr5:139452685 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1917T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452685 | |||||||
| chr5:139452686 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1916T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452686 | |||||||
| chr5:139452687 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1915T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452687 | |||||||
| chr5:139452688 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1914T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452688 | |||||||
| chr5:139452689 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1913T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452689 | |||||||
| chr5:139452690 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1912T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452690 | |||||||
| chr5:139452691 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1911T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452691 | |||||||
| chr5:139452692 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1910T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452692 | |||||||
| chr5:139452693 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1909T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452693 | |||||||
| chr5:139452694 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1908G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452694 | |||||||
| chr5:139452695 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1907T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452695 | |||||||
| chr5:139452696 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1906G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452696 | |||||||
| chr5:139452697 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1905T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452697 | |||||||
| chr5:139452698 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1904T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452698 | |||||||
| chr5:139452699 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1903T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452699 | |||||||
| chr5:139452700 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1902T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452700 | |||||||
| chr5:139452701 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1901T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452701 | |||||||
| chr5:139452702 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1900T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452702 | |||||||
| chr5:139452703 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1899T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452703 | |||||||
| chr5:139452704 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1898G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452704 | |||||||
| chr5:139452705 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1897T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452705 | |||||||
| chr5:139452706 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1896G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452706 | |||||||
| chr5:139452707 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1895T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452707 | |||||||
| chr5:139452708 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1894T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452708 | |||||||
| chr5:139452709 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1893G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452709 | |||||||
| chr5:139452710 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1892T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452710 | |||||||
| chr5:139452711 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1891T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452711 | |||||||
| chr5:139452712 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1890T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452712 | |||||||
| chr5:139452713 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1889T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452713 | |||||||
| chr5:139452714 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1888T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452714 | |||||||
| chr5:139452715 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1887T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452715 | |||||||
| chr5:139452716 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1886T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452716 | |||||||
| chr5:139452717 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1885T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452717 | |||||||
| chr5:139452718 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1884T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452718 | |||||||
| chr5:139452719 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1883T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452719 | |||||||
| chr5:139452720 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1882T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452720 | |||||||
| chr5:139452721 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1881T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452721 | |||||||
| chr5:139452722 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1880T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452722 | |||||||
| chr5:139452723 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1879T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452723 | |||||||
| chr5:139452724 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1878T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452724 | |||||||
| chr5:139452725 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1877T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452725 | |||||||
| chr5:139452726 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1876T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452726 | |||||||
| chr5:139452727 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1875G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452727 | |||||||
| chr5:139452728 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1874T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452728 | |||||||
| chr5:139452729 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1873G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452729 | |||||||
| chr5:139452730 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1872T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452730 | |||||||
| chr5:139452731 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1871T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452731 | |||||||
| chr5:139452732 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1870G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452732 | |||||||
| chr5:139452733 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1869T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452733 | |||||||
| chr5:139452734 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1868G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452734 | |||||||
| chr5:139452735 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1867T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452735 | |||||||
| chr5:139452736 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1866T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452736 | |||||||
| chr5:139452737 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1865T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452737 | |||||||
| chr5:139452738 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1864T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452738 | |||||||
| chr5:139452739 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1863T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452739 | |||||||
| chr5:139452740 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1862T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452740 | |||||||
| chr5:139452741 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1861T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452741 | |||||||
| chr5:139452742 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1860T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452742 | |||||||
| chr5:139452743 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1859T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452743 | |||||||
| chr5:139452744 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1858T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452744 | |||||||
| chr5:139452745 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1857T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452745 | |||||||
| chr5:139452746 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1856T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452746 | |||||||
| chr5:139452747 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1855T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452747 | |||||||
| chr5:139452748 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1854T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452748 | |||||||
| chr5:139452749 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1853T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452749 | |||||||
| chr5:139452750 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1852T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452750 | |||||||
| chr5:139452751 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1851T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452751 | |||||||
| chr5:139452752 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1850T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452752 | |||||||
| chr5:139452753 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1849T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452753 | |||||||
| chr5:139452754 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1848T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452754 | |||||||
| chr5:139452755 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1847T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452755 | |||||||
| chr5:139452756 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1846T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452756 | |||||||
| chr5:139452757 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1845T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452757 | |||||||
| chr5:139452758 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1844T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452758 | |||||||
| chr5:139452759 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1843G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452759 | |||||||
| chr5:139452760 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1842T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452760 | |||||||
| chr5:139452761 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1841T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452761 | |||||||
| chr5:139452762 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1840T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452762 | |||||||
| chr5:139452763 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1839T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452763 | |||||||
| chr5:139452764 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1838G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452764 | |||||||
| chr5:139452765 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1837T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452765 | |||||||
| chr5:139452766 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1836T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452766 | |||||||
| chr5:139452767 | N | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1835T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452767 | |||||||
| chr5:139452768 | N | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1834T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452768 | |||||||
| chr5:139452769 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1833T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452769 | |||||||
| chr5:139452770 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1832T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452770 | |||||||
| chr5:139452771 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1831T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452771 | |||||||
| chr5:139452772 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1830T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452772 | |||||||
| chr5:139452773 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1829T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452773 | |||||||
| chr5:139452774 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1828T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452774 | |||||||
| chr5:139452775 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1827T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452775 | |||||||
| chr5:139452776 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1826T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452776 | |||||||
| chr5:139452777 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1825G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452777 | |||||||
| chr5:139452778 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1824T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452778 | |||||||
| chr5:139452779 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1823T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452779 | |||||||
| chr5:139452780 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1822T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452780 | |||||||
| chr5:139452781 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1821T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452781 | |||||||
| chr5:139452782 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1820G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452782 | |||||||
| chr5:139452783 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1819T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452783 | |||||||
| chr5:139452784 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1818T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452784 | |||||||
| chr5:139452785 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1817T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452785 | |||||||
| chr5:139452786 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1816T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452786 | |||||||
| chr5:139452787 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1815T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452787 | |||||||
| chr5:139452788 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1814T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452788 | |||||||
| chr5:139452789 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1813T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452789 | |||||||
| chr5:139452790 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1812T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452790 | |||||||
| chr5:139452791 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1811T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452791 | |||||||
| chr5:139452792 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1810T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452792 | |||||||
| chr5:139452793 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1809T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452793 | |||||||
| chr5:139452794 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1808T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452794 | |||||||
| chr5:139452795 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1807T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452795 | |||||||
| chr5:139452796 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1806G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452796 | |||||||
| chr5:139452797 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1805T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452797 | |||||||
| chr5:139452798 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1804T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452798 | |||||||
| chr5:139452799 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1803T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452799 | |||||||
| chr5:139452800 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1802T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452800 | |||||||
| chr5:139452801 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1801T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452801 | |||||||
| chr5:139452802 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1800T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452802 | |||||||
| chr5:139452803 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1799T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452803 | |||||||
| chr5:139452804 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1798G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452804 | |||||||
| chr5:139452805 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1797T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452805 | |||||||
| chr5:139452806 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1796G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452806 | |||||||
| chr5:139452807 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1795T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452807 | |||||||
| chr5:139452808 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1794T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452808 | |||||||
| chr5:139452809 | N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1793G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452809 | |||||||
| chr5:139452810 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1792T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452810 | |||||||
| chr5:139452811 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1791T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452811 | |||||||
| chr5:139452812 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1790T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452812 | |||||||
| chr5:139452813 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1789T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452813 | |||||||
| chr5:139452814 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1788T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452814 | |||||||
| chr5:139452815 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1787T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452815 | |||||||
| chr5:139452816 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1786T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452816 | |||||||
| chr5:139452817 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1785T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452817 | |||||||
| chr5:139452818 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1784T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452818 | |||||||
| chr5:139452819 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1783T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452819 | |||||||
| chr5:139452820 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1782T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452820 | |||||||
| chr5:139452821 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1781T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452821 | |||||||
| chr5:139452822 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1780T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452822 | |||||||
| chr5:139452823 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1779T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452823 | |||||||
| chr5:139452824 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1778T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452824 | |||||||
| chr5:139452825 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1777T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452825 | |||||||
| chr5:139452826 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1776T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452826 | |||||||
| chr5:139452827 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1775T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452827 | |||||||
| chr5:139452828 | N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1774T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452828 | |||||||
| chr5:139452829 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1773T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452829 | |||||||
| chr5:139452830 | N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1772T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452830 | |||||||
| chr5:139452831 | NNNNNNNN others(839): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+925_512+1771de others(852): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452831 | |||||||
| chr5:139453357 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1245G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453357 | |||||||
| chr5:139453358 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1244T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453358 | |||||||
| chr5:139453359 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1243T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453359 | |||||||
| chr5:139453360 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1242T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453360 | |||||||
| chr5:139453361 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1241T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453361 | |||||||
| chr5:139453362 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1240T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453362 | |||||||
| chr5:139453363 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1239T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453363 | |||||||
| chr5:139453364 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1238T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453364 | |||||||
| chr5:139453365 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1237T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453365 | |||||||
| chr5:139453366 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1236T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453366 | |||||||
| chr5:139453367 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1235T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453367 | |||||||
| chr5:139453368 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1234G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453368 | |||||||
| chr5:139453369 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1233T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453369 | |||||||
| chr5:139453370 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1232T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453370 | |||||||
| chr5:139453371 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1231T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453371 | |||||||
| chr5:139453372 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1230T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453372 | |||||||
| chr5:139453373 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1229T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453373 | |||||||
| chr5:139453374 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1228T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453374 | |||||||
| chr5:139453375 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1227T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453375 | |||||||
| chr5:139453376 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1226G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453376 | |||||||
| chr5:139453377 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1225T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453377 | |||||||
| chr5:139453378 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1224T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453378 | |||||||
| chr5:139453379 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1223T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453379 | |||||||
| chr5:139453380 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1222T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453380 | |||||||
| chr5:139453381 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1221T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453381 | |||||||
| chr5:139453382 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1220T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453382 | |||||||
| chr5:139453383 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1219T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453383 | |||||||
| chr5:139453384 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1218T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453384 | |||||||
| chr5:139453385 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1217T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453385 | |||||||
| chr5:139453386 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1216T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453386 | |||||||
| chr5:139453387 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1215T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453387 | |||||||
| chr5:139453388 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1214T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453388 | |||||||
| chr5:139453389 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1213T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453389 | |||||||
| chr5:139453390 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1212T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453390 | |||||||
| chr5:139453391 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1211G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453391 | |||||||
| chr5:139453392 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1210T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453392 | |||||||
| chr5:139453393 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1209G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453393 | |||||||
| chr5:139453394 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1208T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453394 | |||||||
| chr5:139453395 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1207T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453395 | |||||||
| chr5:139453396 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1206T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453396 | |||||||
| chr5:139453397 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1205G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453397 | |||||||
| chr5:139453397 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1205T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453397 | |||||||
| chr5:139453398 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1204T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453398 | |||||||
| chr5:139453398 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1204T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453398 | |||||||
| chr5:139453399 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1203T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453399 | |||||||
| chr5:139453400 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1202T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453400 | |||||||
| chr5:139453400 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1202T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453400 | |||||||
| chr5:139453401 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1201G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453401 | |||||||
| chr5:139453401 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1201T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453401 | |||||||
| chr5:139453402 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1200T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453402 | |||||||
| chr5:139453402 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1200T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453402 | |||||||
| chr5:139453403 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1199G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453403 | |||||||
| chr5:139453403 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1199T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453403 | |||||||
| chr5:139453404 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1198T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453404 | |||||||
| chr5:139453405 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1197G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | |||||||
| chr5:139453405 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1197T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | |||||||
| chr5:139453405 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1197T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | |||||||
| chr5:139453406 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1196G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453406 | |||||||
| chr5:139453406 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1196T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453406 | |||||||
| chr5:139453407 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1195T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453407 | |||||||
| chr5:139453407 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1195T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453407 | |||||||
| chr5:139453408 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1194G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453408 | |||||||
| chr5:139453408 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1194T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453408 | |||||||
| chr5:139453409 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1193T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453409 | |||||||
| chr5:139453409 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1193T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453409 | |||||||
| chr5:139453410 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1192T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453410 | |||||||
| chr5:139453410 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1192T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453410 | |||||||
| chr5:139453411 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1191T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453411 | |||||||
| chr5:139453411 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1191T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453411 | |||||||
| chr5:139453412 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1190T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453412 | |||||||
| chr5:139453412 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1190T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453412 | |||||||
| chr5:139453413 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1189T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453413 | |||||||
| chr5:139453414 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1188T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453414 | |||||||
| chr5:139453414 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1188T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453414 | |||||||
| chr5:139453415 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1187T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453415 | |||||||
| chr5:139453415 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1187T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453415 | |||||||
| chr5:139453416 | N | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1186G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453416 | |||||||
| chr5:139453416 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1186T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453416 | |||||||
| chr5:139453417 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1185T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453417 | |||||||
| chr5:139453418 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1184T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453418 | |||||||
| chr5:139453418 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1184T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453418 | |||||||
| chr5:139453419 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1183T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453419 | |||||||
| chr5:139453419 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1183T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453419 | |||||||
| chr5:139453420 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1182T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453420 | |||||||
| chr5:139453421 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1181T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453421 | |||||||
| chr5:139453421 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1181T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453421 | |||||||
| chr5:139453422 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1180T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453422 | |||||||
| chr5:139453423 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1179T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453423 | |||||||
| chr5:139453424 | N | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1178G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453424 | |||||||
| chr5:139453424 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1178T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453424 | |||||||
| chr5:139453425 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1177T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453425 | |||||||
| chr5:139453425 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1177T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453425 | |||||||
| chr5:139453426 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1176G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | |||||||
| chr5:139453426 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1176T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | |||||||
| chr5:139453426 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1176T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | |||||||
| chr5:139453427 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1175T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453427 | |||||||
| chr5:139453427 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1175T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453427 | |||||||
| chr5:139453428 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1174T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453428 | |||||||
| chr5:139453428 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1174T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453428 | |||||||
| chr5:139453429 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1173G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | |||||||
| chr5:139453429 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1173T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | |||||||
| chr5:139453429 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1173T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | |||||||
| chr5:139453430 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1172T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453430 | |||||||
| chr5:139453430 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1172T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453430 | |||||||
| chr5:139453431 | N | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1171G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453431 | |||||||
| chr5:139453431 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1171T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453431 | |||||||
| chr5:139453432 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1170T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453432 | |||||||
| chr5:139453432 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1170T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453432 | |||||||
| chr5:139453433 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1169G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453433 | |||||||
| chr5:139453433 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1169T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453433 | |||||||
| chr5:139453434 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1168T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453434 | |||||||
| chr5:139453435 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1167T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453435 | |||||||
| chr5:139453436 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1166T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453436 | |||||||
| chr5:139453437 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1165T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453437 | |||||||
| chr5:139453438 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1164T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453438 | |||||||
| chr5:139453439 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1163G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453439 | |||||||
| chr5:139453439 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1163T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453439 | |||||||
| chr5:139453440 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1162T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453440 | |||||||
| chr5:139453440 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1162T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453440 | |||||||
| chr5:139453441 | N | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1161G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453441 | |||||||
| chr5:139453441 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1161T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453441 | |||||||
| chr5:139453442 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1160T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453442 | |||||||
| chr5:139453442 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1160T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453442 | |||||||
| chr5:139453443 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1159G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | |||||||
| chr5:139453443 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1159T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | |||||||
| chr5:139453443 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1159T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | |||||||
| chr5:139453444 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1158T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453444 | |||||||
| chr5:139453444 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1158T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453444 | |||||||
| chr5:139453445 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1157T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453445 | |||||||
| chr5:139453445 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1157T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453445 | |||||||
| chr5:139453446 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1156G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | |||||||
| chr5:139453446 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1156T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | |||||||
| chr5:139453446 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1156T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | |||||||
| chr5:139453447 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1155T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453447 | |||||||
| chr5:139453447 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1155T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453447 | |||||||
| chr5:139453448 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1154T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453448 | |||||||
| chr5:139453448 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1154T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453448 | |||||||
| chr5:139453449 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1153G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453449 | |||||||
| chr5:139453449 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1153T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453449 | |||||||
| chr5:139453450 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1152T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453450 | |||||||
| chr5:139453450 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1152T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453450 | |||||||
| chr5:139453451 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1151G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453451 | |||||||
| chr5:139453451 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1151T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453451 | |||||||
| chr5:139453452 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1150T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453452 | |||||||
| chr5:139453452 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1150T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453452 | |||||||
| chr5:139453453 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1149T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453453 | |||||||
| chr5:139453453 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1149T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453453 | |||||||
| chr5:139453454 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1148G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453454 | |||||||
| chr5:139453454 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1148T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453454 | |||||||
| chr5:139453455 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1147T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453455 | |||||||
| chr5:139453455 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1147T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453455 | |||||||
| chr5:139453456 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1146G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | |||||||
| chr5:139453456 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1146T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | |||||||
| chr5:139453456 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1146T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | |||||||
| chr5:139453457 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1145T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453457 | |||||||
| chr5:139453457 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1145T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453457 | |||||||
| chr5:139453458 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1144T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453458 | |||||||
| chr5:139453458 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1144T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453458 | |||||||
| chr5:139453459 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1143T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453459 | |||||||
| chr5:139453459 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1143T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453459 | |||||||
| chr5:139453460 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1142T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453460 | |||||||
| chr5:139453460 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1142T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453460 | |||||||
| chr5:139453461 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1141G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453461 | |||||||
| chr5:139453461 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1141T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453461 | |||||||
| chr5:139453462 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1140T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453462 | |||||||
| chr5:139453462 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1140T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453462 | |||||||
| chr5:139453463 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1139T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453463 | |||||||
| chr5:139453463 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1139T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453463 | |||||||
| chr5:139453464 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1138G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | |||||||
| chr5:139453464 | N | C | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1138T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | |||||||
| chr5:139453464 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1138T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | |||||||
| chr5:139453465 | N | C | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1137T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | |||||||
| chr5:139453465 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1137T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | |||||||
| chr5:139453465 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1137T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | |||||||
| chr5:139453466 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1136G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453466 | |||||||
| chr5:139453466 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1136T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453466 | |||||||
| chr5:139453467 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1135T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453467 | |||||||
| chr5:139453467 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1135T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453467 | |||||||
| chr5:139453468 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1134T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453468 | |||||||
| chr5:139453468 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1134T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453468 | |||||||
| chr5:139453469 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1133G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453469 | |||||||
| chr5:139453469 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1133T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453469 | |||||||
| chr5:139453470 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1132T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453470 | |||||||
| chr5:139453470 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1132T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453470 | |||||||
| chr5:139453471 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1131G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453471 | |||||||
| chr5:139453471 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1131T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453471 | |||||||
| chr5:139453472 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1130G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | |||||||
| chr5:139453472 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1130T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | |||||||
| chr5:139453472 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1130T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | |||||||
| chr5:139453473 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1129T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453473 | |||||||
| chr5:139453473 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1129T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453473 | |||||||
| chr5:139453474 | N | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1128G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453474 | |||||||
| chr5:139453474 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1128T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453474 | |||||||
| chr5:139453475 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1127T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453475 | |||||||
| chr5:139453475 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1127T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453475 | |||||||
| chr5:139453476 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1126T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453476 | |||||||
| chr5:139453476 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1126T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453476 | |||||||
| chr5:139453477 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1125G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | |||||||
| chr5:139453477 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1125T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | |||||||
| chr5:139453477 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1125T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | |||||||
| chr5:139453478 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1124T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453478 | |||||||
| chr5:139453478 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1124T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453478 | |||||||
| chr5:139453479 | N | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1123G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453479 | |||||||
| chr5:139453479 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1123T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453479 | |||||||
| chr5:139453480 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1122T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453480 | |||||||
| chr5:139453480 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1122T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453480 | |||||||
| chr5:139453481 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1121T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453481 | |||||||
| chr5:139453482 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1120T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453482 | |||||||
| chr5:139453482 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1120T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453482 | |||||||
| chr5:139453483 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1119T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453483 | |||||||
| chr5:139453483 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1119T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453483 | |||||||
| chr5:139453484 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1118T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453484 | |||||||
| chr5:139453484 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1118T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453484 | |||||||
| chr5:139453485 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1117T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453485 | |||||||
| chr5:139453485 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1117T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453485 | |||||||
| chr5:139453486 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1116T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453486 | |||||||
| chr5:139453486 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1116T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453486 | |||||||
| chr5:139453487 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1115T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453487 | |||||||
| chr5:139453488 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1114T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453488 | |||||||
| chr5:139453488 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1114T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453488 | |||||||
| chr5:139453489 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1113T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453489 | |||||||
| chr5:139453490 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1112T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453490 | |||||||
| chr5:139453490 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1112T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453490 | |||||||
| chr5:139453491 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1111T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453491 | |||||||
| chr5:139453491 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1111T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453491 | |||||||
| chr5:139453492 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1110T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453492 | |||||||
| chr5:139453492 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1110T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453492 | |||||||
| chr5:139453493 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1109G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | |||||||
| chr5:139453493 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1109T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | |||||||
| chr5:139453493 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1109T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | |||||||
| chr5:139453494 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1108T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453494 | |||||||
| chr5:139453494 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1108T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453494 | |||||||
| chr5:139453495 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1107T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453495 | |||||||
| chr5:139453496 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1106G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | |||||||
| chr5:139453496 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1106T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | |||||||
| chr5:139453496 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1106T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | |||||||
| chr5:139453497 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1105T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453497 | |||||||
| chr5:139453497 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1105T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453497 | |||||||
| chr5:139453498 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1104T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453498 | |||||||
| chr5:139453498 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1104T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453498 | |||||||
| chr5:139453499 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1103T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453499 | |||||||
| chr5:139453499 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1103T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453499 | |||||||
| chr5:139453500 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1102T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453500 | |||||||
| chr5:139453500 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1102T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453500 | |||||||
| chr5:139453501 | N | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1101G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453501 | |||||||
| chr5:139453501 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1101T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453501 | |||||||
| chr5:139453502 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1100T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453502 | |||||||
| chr5:139453502 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1100T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453502 | |||||||
| chr5:139453503 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1099G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453503 | |||||||
| chr5:139453503 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1099T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453503 | |||||||
| chr5:139453504 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1098G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | |||||||
| chr5:139453504 | N | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1098T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | |||||||
| chr5:139453504 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1098T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | |||||||
| chr5:139453505 | N | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1097T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453505 | |||||||
| chr5:139453505 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1097T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453505 | |||||||
| chr5:139453506 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1096G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | |||||||
| chr5:139453506 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1096T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | |||||||
| chr5:139453506 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1096T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | |||||||
| chr5:139453507 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1095T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453507 | |||||||
| chr5:139453507 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1095T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453507 | |||||||
| chr5:139453508 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1094T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453508 | |||||||
| chr5:139453508 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1094T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453508 | |||||||
| chr5:139453509 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1093G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453509 | |||||||
| chr5:139453509 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1093T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453509 | |||||||
| chr5:139453510 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1092T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453510 | |||||||
| chr5:139453511 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1091T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453511 | |||||||
| chr5:139453511 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1091T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453511 | |||||||
| chr5:139453512 | N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1090T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | |||||||
| chr5:139453512 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1090T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | |||||||
| chr5:139453512 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1090T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | |||||||
| chr5:139453513 | N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1089T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | |||||||
| chr5:139453513 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1089T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | |||||||
| chr5:139453513 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1089T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | |||||||
| chr5:139453514 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1088G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453514 | |||||||
| chr5:139453514 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1088T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453514 | |||||||
| chr5:139453515 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1087T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453515 | |||||||
| chr5:139453515 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1087T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453515 | |||||||
| chr5:139453516 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1086T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453516 | |||||||
| chr5:139453517 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1085T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453517 | |||||||
| chr5:139453517 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1085T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453517 | |||||||
| chr5:139453518 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1084T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453518 | |||||||
| chr5:139453518 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1084T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453518 | |||||||
| chr5:139453519 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1083G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | |||||||
| chr5:139453519 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1083T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | |||||||
| chr5:139453519 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1083T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | |||||||
| chr5:139453520 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1082T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453520 | |||||||
| chr5:139453521 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1081T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453521 | |||||||
| chr5:139453521 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1081T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453521 | |||||||
| chr5:139453522 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1080G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453522 | |||||||
| chr5:139453522 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1080T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453522 | |||||||
| chr5:139453523 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1079T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453523 | |||||||
| chr5:139453523 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1079T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453523 | |||||||
| chr5:139453524 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1078T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453524 | |||||||
| chr5:139453524 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1078T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453524 | |||||||
| chr5:139453525 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1077T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453525 | |||||||
| chr5:139453525 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1077T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453525 | |||||||
| chr5:139453526 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1076T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453526 | |||||||
| chr5:139453526 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1076T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453526 | |||||||
| chr5:139453527 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1075G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453527 | |||||||
| chr5:139453527 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1075T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453527 | |||||||
| chr5:139453528 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1074T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453528 | |||||||
| chr5:139453528 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1074T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453528 | |||||||
| chr5:139453529 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1073T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453529 | |||||||
| chr5:139453530 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1072T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453530 | |||||||
| chr5:139453531 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1071T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453531 | |||||||
| chr5:139453532 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1070T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453532 | |||||||
| chr5:139453532 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1070T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453532 | |||||||
| chr5:139453533 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1069G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453533 | |||||||
| chr5:139453533 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1069T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453533 | |||||||
| chr5:139453534 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1068T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453534 | |||||||
| chr5:139453534 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1068T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453534 | |||||||
| chr5:139453535 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1067T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453535 | |||||||
| chr5:139453535 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1067T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453535 | |||||||
| chr5:139453536 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1066T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453536 | |||||||
| chr5:139453536 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1066T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453536 | |||||||
| chr5:139453537 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1065T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453537 | |||||||
| chr5:139453537 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1065T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453537 | |||||||
| chr5:139453538 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1064T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453538 | |||||||
| chr5:139453538 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1064T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453538 | |||||||
| chr5:139453539 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1063T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453539 | |||||||
| chr5:139453539 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1063T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453539 | |||||||
| chr5:139453540 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1062T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453540 | |||||||
| chr5:139453540 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1062T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453540 | |||||||
| chr5:139453541 | N | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1061G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453541 | |||||||
| chr5:139453541 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1061T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453541 | |||||||
| chr5:139453542 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1060T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453542 | |||||||
| chr5:139453542 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1060T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453542 | |||||||
| chr5:139453543 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1059G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | |||||||
| chr5:139453543 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1059T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | |||||||
| chr5:139453543 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1059T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | |||||||
| chr5:139453544 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1058G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453544 | |||||||
| chr5:139453544 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1058T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453544 | |||||||
| chr5:139453545 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1057T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453545 | |||||||
| chr5:139453545 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1057T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453545 | |||||||
| chr5:139453546 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1056G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | |||||||
| chr5:139453546 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1056T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | |||||||
| chr5:139453546 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1056T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | |||||||
| chr5:139453547 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1055T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453547 | |||||||
| chr5:139453547 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1055T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453547 | |||||||
| chr5:139453548 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1054T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453548 | |||||||
| chr5:139453548 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1054T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453548 | |||||||
| chr5:139453549 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1053G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | |||||||
| chr5:139453549 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1053T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | |||||||
| chr5:139453549 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1053T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | |||||||
| chr5:139453550 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1052T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453550 | |||||||
| chr5:139453550 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1052T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453550 | |||||||
| chr5:139453551 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1051G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | |||||||
| chr5:139453551 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1051T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | |||||||
| chr5:139453551 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1051T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | |||||||
| chr5:139453552 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1050T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453552 | |||||||
| chr5:139453552 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1050T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453552 | |||||||
| chr5:139453553 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1049T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453553 | |||||||
| chr5:139453553 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1049T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453553 | |||||||
| chr5:139453554 | N | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1048G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453554 | |||||||
| chr5:139453554 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1048T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453554 | |||||||
| chr5:139453555 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1047T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453555 | |||||||
| chr5:139453555 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1047T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453555 | |||||||
| chr5:139453556 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1046T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453556 | |||||||
| chr5:139453556 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1046T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453556 | |||||||
| chr5:139453557 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1045T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453557 | |||||||
| chr5:139453558 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1044T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453558 | |||||||
| chr5:139453558 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1044T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453558 | |||||||
| chr5:139453559 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1043T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453559 | |||||||
| chr5:139453560 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1042T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453560 | |||||||
| chr5:139453560 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1042T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453560 | |||||||
| chr5:139453561 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1041T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453561 | |||||||
| chr5:139453561 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1041T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453561 | |||||||
| chr5:139453562 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1040T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453562 | |||||||
| chr5:139453562 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1040T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453562 | |||||||
| chr5:139453563 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1039T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453563 | |||||||
| chr5:139453563 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1039T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453563 | |||||||
| chr5:139453564 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1038T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453564 | |||||||
| chr5:139453564 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1038T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453564 | |||||||
| chr5:139453565 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1037T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453565 | |||||||
| chr5:139453565 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1037T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453565 | |||||||
| chr5:139453566 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1036T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453566 | |||||||
| chr5:139453566 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1036T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453566 | |||||||
| chr5:139453567 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1035T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453567 | |||||||
| chr5:139453568 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1034G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453568 | |||||||
| chr5:139453568 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1034T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453568 | |||||||
| chr5:139453569 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1033T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453569 | |||||||
| chr5:139453569 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1033T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453569 | |||||||
| chr5:139453570 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1032T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453570 | |||||||
| chr5:139453571 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1031T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453571 | |||||||
| chr5:139453571 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1031T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453571 | |||||||
| chr5:139453572 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1030T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453572 | |||||||
| chr5:139453572 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1030T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453572 | |||||||
| chr5:139453573 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1029T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453573 | |||||||
| chr5:139453573 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1029T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453573 | |||||||
| chr5:139453574 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1028T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453574 | |||||||
| chr5:139453574 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1028T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453574 | |||||||
| chr5:139453575 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1027T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453575 | |||||||
| chr5:139453575 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1027T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453575 | |||||||
| chr5:139453576 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1026T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453576 | |||||||
| chr5:139453576 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1026T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453576 | |||||||
| chr5:139453577 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1025T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453577 | |||||||
| chr5:139453577 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1025T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453577 | |||||||
| chr5:139453578 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1024T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453578 | |||||||
| chr5:139453578 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1024T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453578 | |||||||
| chr5:139453579 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1023T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453579 | |||||||
| chr5:139453579 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1023T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453579 | |||||||
| chr5:139453580 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1022T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453580 | |||||||
| chr5:139453580 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1022T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453580 | |||||||
| chr5:139453581 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1021T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453581 | |||||||
| chr5:139453581 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1021T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453581 | |||||||
| chr5:139453582 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1020T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453582 | |||||||
| chr5:139453583 | N | A | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1019G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453583 | |||||||
| chr5:139453583 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1019T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453583 | |||||||
| chr5:139453584 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1018G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | |||||||
| chr5:139453584 | N | C | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1018T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | |||||||
| chr5:139453584 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1018T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | |||||||
| chr5:139453585 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1017T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453585 | |||||||
| chr5:139453585 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1017T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453585 | |||||||
| chr5:139453586 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1016T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453586 | |||||||
| chr5:139453586 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1016T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453586 | |||||||
| chr5:139453587 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1015T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453587 | |||||||
| chr5:139453587 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1015T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453587 | |||||||
| chr5:139453588 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1014T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453588 | |||||||
| chr5:139453588 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1014T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453588 | |||||||
| chr5:139453589 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1013T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453589 | |||||||
| chr5:139453589 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1013T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453589 | |||||||
| chr5:139453590 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1012T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453590 | |||||||
| chr5:139453591 | N | G | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1011T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453591 | |||||||
| chr5:139453591 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1011T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453591 | |||||||
| chr5:139453592 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1010G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453592 | |||||||
| chr5:139453592 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1010T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453592 | |||||||
| chr5:139453593 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1009T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453593 | |||||||
| chr5:139453594 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1008G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453594 | |||||||
| chr5:139453594 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1008T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453594 | |||||||
| chr5:139453595 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1007T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453595 | |||||||
| chr5:139453595 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1007T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453595 | |||||||
| chr5:139453596 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1006T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453596 | |||||||
| chr5:139453596 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1006T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453596 | |||||||
| chr5:139453597 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1005T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453597 | |||||||
| chr5:139453597 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1005T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453597 | |||||||
| chr5:139453598 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1004T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453598 | |||||||
| chr5:139453598 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1004T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453598 | |||||||
| chr5:139453599 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1003T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453599 | |||||||
| chr5:139453599 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1003T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453599 | |||||||
| chr5:139453600 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1002T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453600 | |||||||
| chr5:139453601 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1001T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453601 | |||||||
| chr5:139453601 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1001T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453601 | |||||||
| chr5:139453602 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1000G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | |||||||
| chr5:139453602 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+1000T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | |||||||
| chr5:139453602 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1000T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | |||||||
| chr5:139453603 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+999T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453603 | |||||||
| chr5:139453603 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+999T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453603 | |||||||
| chr5:139453604 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+998T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453604 | |||||||
| chr5:139453604 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+998T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453604 | |||||||
| chr5:139453605 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+997T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453605 | |||||||
| chr5:139453605 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+997T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453605 | |||||||
| chr5:139453606 | N | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+996T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453606 | |||||||
| chr5:139453606 | N | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+996T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453606 | |||||||
| chr5:139453607 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+995T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453607 | |||||||
| chr5:139453608 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+994G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453608 | |||||||
| chr5:139453608 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+994T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453608 | |||||||
| chr5:139453609 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+993T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453609 | |||||||
| chr5:139453610 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+992T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453610 | |||||||
| chr5:139453610 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+992T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453610 | |||||||
| chr5:139453611 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+991T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453611 | |||||||
| chr5:139453611 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+991T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453611 | |||||||
| chr5:139453612 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+990T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453612 | |||||||
| chr5:139453612 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+990T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453612 | |||||||
| chr5:139453613 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+989T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453613 | |||||||
| chr5:139453613 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+989T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453613 | |||||||
| chr5:139453614 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+988T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453614 | |||||||
| chr5:139453614 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+988T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453614 | |||||||
| chr5:139453615 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+987T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453615 | |||||||
| chr5:139453616 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+986G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453616 | |||||||
| chr5:139453616 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+986T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453616 | |||||||
| chr5:139453617 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+985T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453617 | |||||||
| chr5:139453617 | N | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+985T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453617 | |||||||
| chr5:139453618 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+984T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453618 | |||||||
| chr5:139453618 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+984T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453618 | |||||||
| chr5:139453619 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+983T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453619 | |||||||
| chr5:139453619 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+983T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453619 | |||||||
| chr5:139453620 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+982T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453620 | |||||||
| chr5:139453620 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+982T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453620 | |||||||
| chr5:139453621 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+981T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453621 | |||||||
| chr5:139453621 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+981T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453621 | |||||||
| chr5:139453622 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+980T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453622 | |||||||
| chr5:139453622 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+980T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453622 | |||||||
| chr5:139453623 | N | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+979G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | |||||||
| chr5:139453623 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+979T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | |||||||
| chr5:139453623 | N | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+979T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | |||||||
| chr5:139453624 | N | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.512+978T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453624 | |||||||
| chr5:139453624 | N | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+978T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453624 | |||||||
| chr5:139453625 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+977T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453625 | |||||||
| chr5:139453625 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+977T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453625 | |||||||
| chr5:139453626 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+976T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453626 | |||||||
| chr5:139453626 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+976T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453626 | |||||||
| chr5:139453627 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+975T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453627 | |||||||
| chr5:139453627 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+975T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453627 | |||||||
| chr5:139453628 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+974T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453628 | |||||||
| chr5:139453628 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+974T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453628 | |||||||
| chr5:139453629 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+973T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453629 | |||||||
| chr5:139453629 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+973T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453629 | |||||||
| chr5:139453630 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+972T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453630 | |||||||
| chr5:139453631 | N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+971G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453631 | |||||||
| chr5:139453631 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+971T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453631 | |||||||
| chr5:139453632 | N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+970T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453632 | |||||||
| chr5:139453632 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+970T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453632 | |||||||
| chr5:139453633 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+969T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453633 | |||||||
| chr5:139453633 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+969T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453633 | |||||||
| chr5:139453634 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+968T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453634 | |||||||
| chr5:139453634 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+968T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453634 | |||||||
| chr5:139453635 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+967T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453635 | |||||||
| chr5:139453635 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+967T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453635 | |||||||
| chr5:139453636 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+966T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453636 | |||||||
| chr5:139453636 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+966T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453636 | |||||||
| chr5:139453637 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+965T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453637 | |||||||
| chr5:139453637 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+965T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453637 | |||||||
| chr5:139453638 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+964T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453638 | |||||||
| chr5:139453639 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+963T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453639 | |||||||
| chr5:139453639 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+963T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453639 | |||||||
| chr5:139453640 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+962T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453640 | |||||||
| chr5:139453641 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+961T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453641 | |||||||
| chr5:139453641 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+961T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453641 | |||||||
| chr5:139453642 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+960T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453642 | |||||||
| chr5:139453642 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+960T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453642 | |||||||
| chr5:139453643 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+959T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453643 | |||||||
| chr5:139453643 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+959T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453643 | |||||||
| chr5:139453644 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+958T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453644 | |||||||
| chr5:139453644 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+958T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453644 | |||||||
| chr5:139453645 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+957T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453645 | |||||||
| chr5:139453645 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+957T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453645 | |||||||
| chr5:139453646 | N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+956T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453646 | |||||||
| chr5:139453646 | N | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+956T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453646 | |||||||
| chr5:139453647 | N | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+955T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453647 | |||||||
| chr5:139453647 | N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+955T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453647 | |||||||
| chr5:139453648 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+954T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453648 | |||||||
| chr5:139453649 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+953T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453649 | |||||||
| chr5:139453650 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+952T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453650 | |||||||
| chr5:139453651 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+951T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453651 | |||||||
| chr5:139453652 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+950T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453652 | |||||||
| chr5:139453653 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+949T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453653 | |||||||
| chr5:139453654 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+948T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453654 | |||||||
| chr5:139453655 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+947T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453655 | |||||||
| chr5:139453656 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+946T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453656 | |||||||
| chr5:139453657 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+945T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453657 | |||||||
| chr5:139453658 | N | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+944T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453658 | |||||||
| chr5:139453659 | N | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+943T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453659 | |||||||
| chr5:139453680 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+922T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453680 | |||||||
| chr5:139453684 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+918C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453684 | |||||||
| chr5:139453687 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+915C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453687 | |||||||
| chr5:139453690 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+912A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453690 | |||||||
| chr5:139453697 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+905A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453697 | |||||||
| chr5:139453700 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+902C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453700 | |||||||
| chr5:139453703 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+899T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453703 | |||||||
| chr5:139453704 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+898A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453704 | |||||||
| chr5:139453725 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+877T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453725 | |||||||
| chr5:139453730 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+872A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453730 | |||||||
| chr5:139453731 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+871T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453731 | |||||||
| chr5:139453731 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+871T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453731 | |||||||
| chr5:139453737 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+865C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453737 | |||||||
| chr5:139453744 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+858C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453744 | |||||||
| chr5:139453744 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+858C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453744 | |||||||
| chr5:139453745 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+857C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453745 | |||||||
| chr5:139453746 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+856C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453746 | |||||||
| chr5:139453747 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+855T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453747 | |||||||
| chr5:139453756 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+846A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453756 | |||||||
| chr5:139453759 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+843A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453759 | |||||||
| chr5:139453763 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+839C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453763 | |||||||
| chr5:139453765 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+837A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453765 | |||||||
| chr5:139453773 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+829A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453773 | |||||||
| chr5:139453775 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+827A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453775 | |||||||
| chr5:139453776 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+826C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453776 | |||||||
| chr5:139453777 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+825C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453777 | |||||||
| chr5:139453789 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+813G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453789 | |||||||
| chr5:139453790 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+812T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453790 | |||||||
| chr5:139453799 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+803C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453799 | |||||||
| chr5:139453846 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+756A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453846 | |||||||
| chr5:139453847 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+755T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453847 | |||||||
| chr5:139453853 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+749C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453853 | |||||||
| chr5:139453865 | TGTGGTGT others(7): Show |
T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+723_512+736del others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453865 | |||||||
| chr5:139454064 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.512+538C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454064 | |||||||
| chr5:139454239 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.512+363G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454239 | |||||||
| chr5:139454259 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.512+343G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454259 | |||||||
| chr5:139454378 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.512+224A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454378 | |||||||
| chr5:139454418 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.512+184C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454418 | |||||||
| chr5:139454544 | G | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0143 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.512+58C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454544 | |||||||
| chr5:139454593 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+9G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454593 | |||||||
| chr5:139454929 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp2 | splice_region_variant&intron_variant | LOW | c.377-6G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454929 | |||||||
| chr5:139454978 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.377-55T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454978 | |||||||
| chr5:139454988 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.377-65G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454988 | |||||||
| chr5:139455650 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.263-214A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455650 | |||||||
| chr5:139455766 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.263-330G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455766 | |||||||
| chr5:139455814 | T | TA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(62): Show |
160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.263-379dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | |||||||
| chr5:139455814 | T | TAA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0040 others(12): Show |
28 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.263-380_263-379dup others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | |||||||
| chr5:139455814 | T | TAAAA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(11): Show |
20 | HG02129.hp1 HG02723.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.263-382_263-379dup others(4): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | |||||||
| chr5:139455814 | T | TAAAAA | 6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0054 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-383_263-379dup others(5): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | |||||||
| chr5:139455814 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.263-392_263-379del others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | |||||||
| chr5:139455883 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.263-447C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455883 | |||||||
| chr5:139456117 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.262+357C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456117 | |||||||
| chr5:139456187 | C | CA | 2 | a0001c0001t0001g0035 a0001c0001t0001g0109 |
3 | NA18965.hp1 NA19004.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.262+286dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456187 | |||||||
| chr5:139456204 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG00673.hp1 HG02129.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+270T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456204 | |||||||
| chr5:139456211 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0065 others(2): Show |
8 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+263G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456211 | |||||||
| chr5:139456267 | A | G | 1 | a0001c0001t0001g0006 | 5 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+207T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456267 | |||||||
| chr5:139456273 | A | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0143 |
3 | HG01891.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.262+201T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456273 | |||||||
| chr5:139456327 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262+147A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456327 | |||||||
| chr5:139456440 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.262+34C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456440 | |||||||
| chr5:139456464 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.262+10G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456464 | |||||||
| chr5:139457068 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG00280.hp2 HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.217+477C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457068 | |||||||
| chr5:139457282 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.217+263G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457282 | |||||||
| chr5:139457294 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.217+251C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457294 | |||||||
| chr5:139457384 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.217+161G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457384 | |||||||
| chr5:139457485 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0116 |
5 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+60G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457485 | |||||||
| chr5:139458045 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106+94G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 2/9 | chr5 | 139458045 | |||||||
| chr5:139458317 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-134A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458317 | |||||||
| chr5:139458320 | G | GT | 3 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0063 |
7 | HG02145.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-138dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458320 | |||||||
| chr5:139458324 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-141A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458324 | |||||||
| chr5:139458325 | G | GT | 22 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
28 | HG00733.hp2 HG01243.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.62-143dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458325 | |||||||
| chr5:139458325 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0063 others(2): Show |
9 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-142C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458325 | |||||||
| chr5:139458330 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0041 |
4 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-147A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458330 | |||||||
| chr5:139458472 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.62-289A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458472 | |||||||
| chr5:139458484 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0138 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-301C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458484 | |||||||
| chr5:139458489 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.62-306G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458489 | |||||||
| chr5:139458500 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-329_62-318dupTT others(10): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG01069.hp1 HG02523.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-330_62-318dupTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
7 | HG01071.hp2 HG01358.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-331_62-318dupTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0142 a0002c0002t0001g0141 |
2 | HG02280.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.62-332_62-318dupTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0143 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-333_62-318dupTT others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0155 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.62-337_62-318dupTT others(18): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAACAAAA others(6): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0131 |
3 | HG01993.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.62-318_62-317insTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAACAAAA others(7): Show |
1 | a0001c0001t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-318_62-317insTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAACAACA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.62-318_62-317insTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAACAACA others(8): Show |
1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62-318_62-317insTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | C | CAACAACA others(11): Show |
1 | a0001c0001t0001g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62-318_62-317insTT others(16): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CA | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0046 others(8): Show |
27 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.62-318delT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAA | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
11 | HG02129.hp1 HG03688.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-319_62-318delTT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAA | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0037 a0001c0001t0001g0055 others(7): Show |
12 | HG01884.hp2 HG02965.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-320_62-318delTT others(1): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(5): Show |
15 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-324_62-318delTT others(5): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
6 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-328_62-318delTT others(9): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18522.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.62-329_62-318delTT others(10): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0052 others(2): Show |
7 | HG02965.hp1 NA18612.hp1 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-330_62-318delTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA others(7): Show |
C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(37): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.62-331_62-318delTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458500 | CAAAAAAA others(8): Show |
C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.62-332_62-318delTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | |||||||
| chr5:139458640 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.62-457T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458640 | |||||||
| chr5:139458771 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-588C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458771 | |||||||
| chr5:139458845 | C | CA | 8 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0037 others(5): Show |
13 | HG01884.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-663dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458845 | |||||||
| chr5:139458861 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.62-678C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458861 | |||||||
| chr5:139459102 | AAACTAGT others(20): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-946_62-920delCT others(25): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459102 | |||||||
| chr5:139459227 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG00597.hp1 HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.62-1044T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459227 | |||||||
| chr5:139459380 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.62-1197G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459380 | |||||||
| chr5:139459452 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.62-1269T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459452 | |||||||
| chr5:139459744 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62-1561G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459744 | |||||||
| chr5:139459769 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62-1586C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459769 | |||||||
| chr5:139459871 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.62-1688T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459871 | |||||||
| chr5:139460110 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.62-1927G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460110 | |||||||
| chr5:139460133 | G | GT | 24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(21): Show |
35 | HG01243.hp2 HG02109.hp1 HG02129.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-1951dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460133 | |||||||
| chr5:139460384 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-2201G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460384 | |||||||
| chr5:139460802 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0150 |
3 | HG01081.hp1 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.61+1808C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460802 | |||||||
| chr5:139461077 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.61+1533C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461077 | |||||||
| chr5:139461244 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1366C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461244 | |||||||
| chr5:139461560 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.61+1050C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461560 | |||||||
| chr5:139461718 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0045 |
3 | HG03490.hp2 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.61+892G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461718 | |||||||
| chr5:139461763 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+847G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461763 | |||||||
| chr5:139461821 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.61+789T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461821 | |||||||
| chr5:139461865 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+745A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461865 | |||||||
| chr5:139461879 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0152 others(3): Show |
11 | HG01074.hp2 HG01081.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+731A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461879 | |||||||
| chr5:139461953 | A | G | 1 | a0001c0001t0001g0009 | 4 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+657T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461953 | |||||||
| chr5:139462071 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.61+539G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462071 | |||||||
| chr5:139462234 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.61+376C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462234 | |||||||
| chr5:139462265 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61+345A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462265 | |||||||
| chr5:139462420 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.61+190C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462420 | |||||||
| chr5:139462593 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0041 |
4 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+17G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462593 |