Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 119559 |
| ensemblid | ENSG00000183605.17 |
| hgncid | 16088 |
| symbol | SFXN4 |
| name | sideroflexin 4 |
| refseq_nuc | NM_213649.2 |
| refseq_prot | NP_998814.1 |
| ensembl_nuc | ENST00000355697.7 |
| ensembl_prot | ENSP00000347924.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 119140767 |
| end | 119165714 |
| strand | - |
| ver | v1.2 |
| region | chr10:119140767-119165714 |
| region5000 | chr10:119135767-119170714 |
| regionname0 | SFXN4_chr10_119140767_119165714 |
| regionname5000 | SFXN4_chr10_119135767_119170714 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 337 | 428 | 93 | 83 | 184 | 18 | 48 | 146 | SFXN4_chr10_119135767_119170714 | SFXN4 | MSLEQ others(332): Show |
chr10 | 119135767 | 119170714 |
| a0002 | 0/0 | 337 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | MSLEQ others(332): Show |
chr10 | 119135767 | 119170714 |
| a0003 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | MSLEQ others(332): Show |
chr10 | 119135767 | 119170714 |
| a0004 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | MSLEQ others(332): Show |
chr10 | 119135767 | 119170714 |
| a0005 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | MSLEQ others(332): Show |
chr10 | 119135767 | 119170714 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1011 | 226 | 34 | 46 | 120 | 9 | 16 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0002 | 0/0 | 1011 | 181 | 43 | 36 | 63 | 9 | 30 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0003 | 1/0 | 1011 | 10 | 9 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0004 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0005 | 0/0 | 1011 | 3 | 2 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0010 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0011 | 0/0 | 1011 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0012 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0001c0013 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0002c0008 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0003c0014 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0004c0007 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 | ||
| a0005c0009 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | ATGTC others(1006): Show |
chr10 | 119135767 | 119170714 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1556 | 187 | 28 | 42 | 91 | 9 | 16 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0001t0002 | 0/0 | 1556 | 35 | 4 | 4 | 27 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0001t0003 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0001t0004 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0001t0007 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0001t0008 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0002t0001 | 0/0 | 1556 | 157 | 29 | 34 | 57 | 9 | 28 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0002t0002 | 0/0 | 1556 | 21 | 11 | 2 | 6 | 0 | 2 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0002t0003 | 0/0 | 1556 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0002t0006 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0003t0001 | 0/0 | 1556 | 7 | 7 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0003t0003 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0003t0004 | 1/0 | 1556 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0003t0005 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0004t0001 | 0/0 | 1556 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0004t0002 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0005t0001 | 0/0 | 1556 | 3 | 2 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0006t0001 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0010t0001 | 0/0 | 1556 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0011t0001 | 0/0 | 1556 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0012t0009 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0001c0013t0001 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0002c0008t0001 | 0/0 | 1556 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0003c0014t0001 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0004c0007t0001 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| a0005c0009t0001 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | GGGGC others(1551): Show |
chr10 | 119135767 | 119170714 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 5 | 5 | 3 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0007g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 1 | 2 | 3 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0008 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0002t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0004g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0004t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0005t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0005t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0005t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0010t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0011t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0012t0009g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0001c0013t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0002c0008t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0003c0014t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0004c0007t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| a0005c0009t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0114 | EUR | GBR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | GBR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00438 | hp1 | a0001 | c0001 | t0008 | g0179 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00741 | hp1 | a0001 | c0010 | t0001 | g0151 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0171 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0113 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0362 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0356 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02148 | hp1 | a0002 | c0008 | t0001 | g0345 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CDX | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0366 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0367 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02280 | hp2 | a0001 | c0013 | t0001 | g0371 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0180 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0372 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0339 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0349 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0368 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0153 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0321 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0370 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0344 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0340 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0363 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0338 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0364 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0347 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0337 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03710 | hp1 | a0001 | c0011 | t0001 | g0283 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0161 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0348 | AFR | YRI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | CHB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19030 | hp2 | a0003 | c0014 | t0001 | g0373 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0346 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0355 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19063 | hp2 | a0004 | c0007 | t0001 | g0361 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19077 | hp1 | a0001 | c0006 | t0001 | g0026 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19078 | hp1 | a0005 | c0009 | t0001 | g0099 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | YRI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | YRI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | ASW | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0106 | EUR | TSI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0369 | SAS | GIH | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02559 | hp1 | a0001 | c0012 | t0009 | g0374 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | MSL | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | USA | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | USA | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | USA | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | USA | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0293 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| NA21309 | hp2 | a0001 | c0003 | t0005 | g0032 | AFR | LWK | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0038 | REF | REF | SFXN4_chr10_119135767_119170714 | SFXN4 | chr10 | 119135767 | 119170714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:119155111 | A | T | 1 | a0005 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.683T>A | p.Met228Lys | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/14 | 750/1556 | 683/1014 | 228/337 | chr10 | 119155111 | |||
| chr10:119157729 | C | T | 1 | a0002 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.476G>A | p.Cys159Tyr | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/14 | 543/1556 | 476/1014 | 159/337 | chr10 | 119157729 | |||
| chr10:119161062 | C | T | 1 | a0003 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.272G>A | p.Arg91Gln | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 4/14 | 339/1556 | 272/1014 | 91/337 | chr10 | 119161062 | |||
| chr10:119164159 | A | G | 1 | a0004 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.149T>C | p.Leu50Ser | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/14 | 216/1556 | 149/1014 | 50/337 | chr10 | 119164159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:119147846 | C | T | 1 | a0001c0011 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.747G>A | p.Thr249Thr | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/14 | 814/1556 | 747/1014 | 249/337 | chr10 | 119147846 | |||
| chr10:119155091 | G | A | 1 | a0001c0012 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.703C>T | p.Leu235Leu | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/14 | 770/1556 | 703/1014 | 235/337 | chr10 | 119155091 | |||
| chr10:119155116 | C | T | 1 | a0001c0004 | 3 | HG02280.hp1 HG02572.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.678G>A | p.Ala226Ala | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/14 | 745/1556 | 678/1014 | 226/337 | chr10 | 119155116 | |||
| chr10:119157871 | G | A | 1 | a0001c0010 | 1 | HG00741.hp1 | splice_region_variant&synonymous_variant | LOW | c.471C>T | p.Tyr157Tyr | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 8/14 | 538/1556 | 471/1014 | 157/337 | chr10 | 119157871 | |||
| chr10:119159734 | T | C | 13 | a0001c0001 a0001c0002 a0001c0004 others(10): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
synonymous_variant | LOW | c.354A>G | p.Ala118Ala | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/14 | 421/1556 | 354/1014 | 118/337 | chr10 | 119159734 | |||
| chr10:119161076 | T | C | 3 | a0001c0001 a0001c0011 a0001c0013 |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
synonymous_variant | LOW | c.258A>G | p.Gln86Gln | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 4/14 | 325/1556 | 258/1014 | 86/337 | chr10 | 119161076 | |||
| chr10:119162388 | T | C | 2 | a0001c0012 a0003c0014 |
2 | HG02559.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.204A>G | p.Leu68Leu | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/14 | 271/1556 | 204/1014 | 68/337 | chr10 | 119162388 | |||
| chr10:119165609 | C | T | 1 | a0001c0006 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.39G>A | p.Arg13Arg | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/14 | 106/1556 | 39/1014 | 13/337 | chr10 | 119165609 | |||
| chr10:119165641 | G | A | 3 | a0001c0005 a0001c0013 a0003c0014 |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.7C>T | p.Leu3Leu | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/14 | 74/1556 | 7/1014 | 3/337 | chr10 | 119165641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:119140808 | T | G | 1 | a0001c0001t0007 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 434 | chr10 | 119140808 | ||||||
| chr10:119140821 | T | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
3_prime_UTR_variant | MODIFIER | c.*421A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 421 | chr10 | 119140821 | ||||||
| chr10:119140986 | C | T | 1 | a0001c0002t0006 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*256G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 256 | chr10 | 119140986 | ||||||
| chr10:119141008 | C | A | 1 | a0001c0001t0008 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 234 | chr10 | 119141008 | ||||||
| chr10:119141037 | C | T | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 |
4 | HG02976.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 205 | chr10 | 119141037 | ||||||
| chr10:119141113 | C | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0002t0002 others(3): Show |
61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 129 | chr10 | 119141113 | ||||||
| chr10:119141181 | C | G | 1 | a0001c0003t0005 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*61G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 14/14 | 61 | chr10 | 119141181 | ||||||
| chr10:119165668 | C | A | 1 | a0001c0012t0009 | 1 | HG02559.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/14 | chr10 | 119165668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:119141464 | AT | A | 117 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0022 others(114): Show |
132 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.937-146delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141464 | |||||||
| chr10:119141464 | ATT | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(234): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.937-147_937-146del others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141464 | |||||||
| chr10:119141507 | C | CT | 105 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0035 others(102): Show |
119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.937-189dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141507 | |||||||
| chr10:119141507 | C | CTT | 11 | a0001c0001t0001g0297 a0001c0001t0001g0316 a0001c0002t0001g0120 others(8): Show |
11 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.937-190_937-189dup others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141507 | |||||||
| chr10:119141507 | CT | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0188 others(18): Show |
22 | HG01070.hp2 HG01167.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.937-189delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141507 | |||||||
| chr10:119141541 | T | G | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.937-222A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141541 | |||||||
| chr10:119141663 | C | T | 2 | a0001c0001t0001g0064 a0001c0002t0001g0126 |
2 | HG01192.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.937-344G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141663 | |||||||
| chr10:119141664 | G | A | 3 | a0001c0003t0001g0344 a0001c0003t0001g0364 a0001c0003t0001g0368 |
3 | HG02886.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.937-345C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141664 | |||||||
| chr10:119141708 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
6 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-389T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141708 | |||||||
| chr10:119141720 | T | C | 10 | a0001c0001t0002g0225 a0001c0001t0002g0322 a0001c0001t0002g0350 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.937-401A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141720 | |||||||
| chr10:119141889 | A | C | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.937-570T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141889 | |||||||
| chr10:119141911 | C | T | 4 | a0001c0001t0002g0341 a0001c0002t0002g0027 a0001c0002t0002g0029 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-592G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119141911 | |||||||
| chr10:119142019 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
6 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-700A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142019 | |||||||
| chr10:119142032 | T | A | 74 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0022 others(71): Show |
85 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.937-713A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142032 | |||||||
| chr10:119142049 | A | C | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.937-730T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142049 | |||||||
| chr10:119142102 | G | T | 58 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(55): Show |
68 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.937-783C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142102 | |||||||
| chr10:119142136 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(12): Show |
17 | HG02004.hp1 HG02165.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.937-817C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142136 | |||||||
| chr10:119142337 | C | A | 3 | a0001c0001t0001g0325 a0001c0001t0001g0343 a0001c0002t0001g0185 |
3 | HG01109.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.937-1018G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142337 | |||||||
| chr10:119142373 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.937-1054G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142373 | |||||||
| chr10:119142412 | T | C | 1 | a0003c0014t0001g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.937-1093A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142412 | |||||||
| chr10:119142451 | A | G | 3 | a0001c0001t0003g0340 a0001c0002t0003g0036 a0001c0002t0003g0037 |
3 | HG02976.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.937-1132T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142451 | |||||||
| chr10:119142546 | C | CT | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(295): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.937-1228dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142546 | |||||||
| chr10:119142546 | C | CTT | 45 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0313 others(42): Show |
49 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.937-1229_937-1228d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142546 | |||||||
| chr10:119142565 | A | T | 371 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(368): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.937-1246T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142565 | |||||||
| chr10:119142619 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.937-1300G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142619 | |||||||
| chr10:119142620 | G | A | 2 | a0001c0002t0001g0095 a0001c0002t0001g0114 |
2 | HG00099.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.937-1301C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142620 | |||||||
| chr10:119142652 | G | A | 2 | a0001c0004t0001g0181 a0001c0005t0001g0372 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.937-1333C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142652 | |||||||
| chr10:119142715 | T | C | 67 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0022 others(64): Show |
78 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.937-1396A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142715 | |||||||
| chr10:119142726 | A | AT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
116 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.937-1408dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142726 | |||||||
| chr10:119142726 | A | ATT | 9 | a0001c0001t0001g0064 a0001c0001t0002g0225 a0001c0001t0008g0179 others(6): Show |
9 | HG00438.hp1 HG00642.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.937-1409_937-1408d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142726 | |||||||
| chr10:119142726 | AT | A | 46 | a0001c0001t0001g0190 a0001c0001t0001g0273 a0001c0001t0001g0299 others(43): Show |
50 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.937-1408delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142726 | |||||||
| chr10:119142726 | ATT | A | 62 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0022 others(59): Show |
73 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.937-1409_937-1408d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142726 | |||||||
| chr10:119142726 | ATTTTTT | A | 6 | a0001c0002t0001g0120 a0001c0002t0006g0153 a0001c0003t0001g0091 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-1413_937-1408d others(8): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142726 | |||||||
| chr10:119142774 | C | A | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.937-1455G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142774 | |||||||
| chr10:119142775 | A | G | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.937-1456T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142775 | |||||||
| chr10:119142877 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.937-1558C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142877 | |||||||
| chr10:119142978 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1659G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119142978 | |||||||
| chr10:119143028 | G | A | 5 | a0001c0001t0001g0325 a0001c0001t0001g0343 a0001c0002t0001g0185 others(2): Show |
5 | HG01109.hp1 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.937-1709C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143028 | |||||||
| chr10:119143080 | T | C | 42 | a0001c0001t0001g0308 a0001c0001t0001g0313 a0001c0001t0002g0009 others(39): Show |
46 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.937-1761A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143080 | |||||||
| chr10:119143151 | A | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG02165.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.937-1832T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143151 | |||||||
| chr10:119143250 | A | G | 1 | a0003c0014t0001g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.937-1931T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143250 | |||||||
| chr10:119143358 | T | C | 1 | a0001c0001t0002g0260 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.937-2039A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143358 | |||||||
| chr10:119143382 | TC | T | 7 | a0001c0001t0001g0352 a0001c0001t0001g0360 a0001c0001t0002g0039 others(4): Show |
7 | HG02717.hp1 HG02976.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-2064delG | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143382 | |||||||
| chr10:119143383 | C | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(362): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.937-2064G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143383 | |||||||
| chr10:119143400 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-2081G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143400 | |||||||
| chr10:119143476 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.937-2157G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143476 | |||||||
| chr10:119143486 | C | A | 2 | a0001c0002t0001g0131 a0001c0002t0001g0141 |
2 | HG01081.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.937-2167G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143486 | |||||||
| chr10:119143618 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.937-2299G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143618 | |||||||
| chr10:119143630 | A | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(111): Show |
128 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.937-2311T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143630 | |||||||
| chr10:119143701 | G | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(278): Show |
321 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.937-2382C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143701 | |||||||
| chr10:119143704 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.937-2385C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143704 | |||||||
| chr10:119143783 | T | G | 1 | a0001c0001t0007g0355 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.936+2453A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143783 | |||||||
| chr10:119143805 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0305 |
2 | NA18967.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.936+2431C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143805 | |||||||
| chr10:119143814 | C | A | 1 | a0001c0002t0001g0137 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.936+2422G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143814 | |||||||
| chr10:119143894 | A | G | 1 | a0001c0002t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.936+2342T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143894 | |||||||
| chr10:119143968 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(10): Show |
14 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.936+2268A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119143968 | |||||||
| chr10:119144034 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.936+2202A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144034 | |||||||
| chr10:119144178 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(16): Show |
20 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.936+2058G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144178 | |||||||
| chr10:119144204 | A | C | 5 | a0001c0001t0001g0143 a0001c0001t0002g0341 a0001c0002t0002g0027 others(2): Show |
5 | HG02630.hp2 HG02735.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+2032T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144204 | |||||||
| chr10:119144227 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(187): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.936+2009G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144227 | |||||||
| chr10:119144272 | T | C | 5 | a0001c0002t0001g0166 a0001c0002t0001g0172 a0001c0002t0001g0176 others(2): Show |
5 | HG01361.hp2 HG01981.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+1964A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144272 | |||||||
| chr10:119144403 | G | T | 1 | a0001c0002t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.936+1833C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144403 | |||||||
| chr10:119144405 | C | T | 10 | a0001c0001t0002g0225 a0001c0001t0002g0322 a0001c0001t0002g0350 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.936+1831G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144405 | |||||||
| chr10:119144435 | T | C | 1 | a0001c0001t0002g0019 | 2 | NA18952.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.936+1801A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144435 | |||||||
| chr10:119144436 | GAC | G | 3 | a0001c0002t0001g0193 a0001c0002t0001g0204 a0001c0002t0001g0211 |
3 | HG01261.hp1 HG01943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.936+1798_936+1799d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144436 | |||||||
| chr10:119144442 | A | G | 1 | a0001c0001t0002g0019 | 2 | NA18952.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.936+1794T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144442 | |||||||
| chr10:119144444 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+1792C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144444 | |||||||
| chr10:119144468 | A | G | 1 | a0001c0002t0001g0108 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.936+1768T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144468 | |||||||
| chr10:119144501 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(154): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.936+1735A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144501 | |||||||
| chr10:119144527 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+1709T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144527 | |||||||
| chr10:119144561 | T | TA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0190 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+1674dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144561 | |||||||
| chr10:119144561 | TA | T | 63 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(60): Show |
73 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.936+1674delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144561 | |||||||
| chr10:119144782 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.936+1454T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144782 | |||||||
| chr10:119144818 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.936+1418T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144818 | |||||||
| chr10:119144821 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.936+1415G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144821 | |||||||
| chr10:119144871 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(90): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.936+1365G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144871 | |||||||
| chr10:119144967 | A | T | 1 | a0001c0001t0001g0285 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.936+1269T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119144967 | |||||||
| chr10:119145001 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.936+1235A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145001 | |||||||
| chr10:119145031 | T | C | 8 | a0001c0001t0002g0341 a0001c0002t0001g0083 a0001c0002t0002g0027 others(5): Show |
8 | HG00408.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.936+1205A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145031 | |||||||
| chr10:119145094 | TATC | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(165): Show |
202 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.936+1139_936+1141d others(5): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145094 | |||||||
| chr10:119145121 | G | A | 69 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0190 others(66): Show |
75 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(72): Show |
intron_variant | MODIFIER | c.936+1115C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145121 | |||||||
| chr10:119145162 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
178 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.936+1074G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145162 | |||||||
| chr10:119145304 | T | TCCTC | 5 | a0001c0002t0002g0027 a0001c0002t0003g0036 a0001c0002t0003g0037 others(2): Show |
5 | HG02572.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+931_936+932ins others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145304 | |||||||
| chr10:119145304 | T | TCTTC | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(353): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.936+931_936+932ins others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145304 | |||||||
| chr10:119145307 | T | TC | 4 | a0001c0003t0001g0033 a0001c0003t0001g0091 a0001c0003t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+928_936+929ins others(1): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145307 | |||||||
| chr10:119145308 | A | C | 4 | a0001c0003t0001g0033 a0001c0003t0001g0091 a0001c0003t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+928T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145308 | |||||||
| chr10:119145310 | G | T | 4 | a0001c0003t0001g0033 a0001c0003t0001g0091 a0001c0003t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+926C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145310 | |||||||
| chr10:119145311 | A | AT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(18): Show |
22 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.936+924dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145311 | |||||||
| chr10:119145311 | AT | A | 31 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0273 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.936+924delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145311 | |||||||
| chr10:119145313 | T | G | 4 | a0001c0003t0001g0033 a0001c0003t0001g0091 a0001c0003t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+923A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145313 | |||||||
| chr10:119145314 | T | A | 4 | a0001c0003t0001g0033 a0001c0003t0001g0091 a0001c0003t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+922A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145314 | |||||||
| chr10:119145418 | G | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0040 others(15): Show |
21 | HG00099.hp1 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.936+818C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145418 | |||||||
| chr10:119145559 | G | A | 1 | a0001c0002t0001g0186 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.936+677C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145559 | |||||||
| chr10:119145702 | G | T | 70 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0250 others(67): Show |
75 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.936+534C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145702 | |||||||
| chr10:119145888 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.936+348A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145888 | |||||||
| chr10:119145910 | T | C | 109 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(106): Show |
124 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.936+326A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145910 | |||||||
| chr10:119145936 | C | T | 2 | a0001c0002t0001g0120 a0001c0002t0001g0292 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.936+300G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119145936 | |||||||
| chr10:119146152 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.936+84T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 13/13 | chr10 | 119146152 | |||||||
| chr10:119146428 | C | CGT | 49 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0002t0001g0008 others(46): Show |
53 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.819-77_819-76dupAC | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146428 | |||||||
| chr10:119146428 | C | CGTGT | 7 | a0001c0002t0001g0025 a0001c0002t0001g0107 a0001c0002t0001g0192 others(4): Show |
8 | HG01496.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-79_819-76dupAC others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146428 | |||||||
| chr10:119146428 | CGTGT | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.819-79_819-76delAC others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146428 | |||||||
| chr10:119146436 | TGTGTGTG others(21): Show |
T | 2 | a0001c0001t0004g0088 a0001c0012t0009g0374 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.819-111_819-84delG others(27): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146436 | |||||||
| chr10:119146454 | T | C | 2 | a0001c0001t0001g0254 a0001c0001t0002g0253 |
2 | HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.819-101A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146454 | |||||||
| chr10:119146455 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0002g0253 |
2 | HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.819-102C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146455 | |||||||
| chr10:119146456 | T | C | 4 | a0001c0001t0001g0254 a0001c0001t0002g0234 a0001c0001t0002g0253 others(1): Show |
4 | HG00738.hp1 HG02486.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-103A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146456 | |||||||
| chr10:119146457 | G | A | 2 | a0001c0001t0002g0234 a0001c0002t0001g0090 |
2 | NA18974.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.819-104C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146457 | |||||||
| chr10:119146458 | T | C | 12 | a0001c0001t0001g0188 a0001c0001t0001g0295 a0001c0001t0001g0302 others(9): Show |
12 | HG01952.hp2 HG01981.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.819-105A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146458 | |||||||
| chr10:119146460 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
116 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.819-107A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGC | 3 | a0001c0002t0001g0094 a0001c0002t0001g0150 a0001c0002t0001g0187 |
3 | HG02723.hp1 HG02723.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.819-109_819-108dup others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGC | 31 | a0001c0001t0001g0245 a0001c0002t0001g0003 a0001c0002t0001g0004 others(28): Show |
37 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.819-108_819-107ins others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGC | 44 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(41): Show |
49 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.819-108_819-107ins others(6): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(1): Show |
11 | a0001c0002t0001g0003 a0001c0002t0001g0050 a0001c0002t0001g0053 others(8): Show |
11 | HG01993.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.819-108_819-107ins others(8): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(3): Show |
1 | a0001c0002t0001g0003 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(10): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(5): Show |
1 | a0001c0002t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(12): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(27): Show |
1 | a0001c0002t0002g0168 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(34): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(29): Show |
1 | a0001c0002t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(36): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(37): Show |
1 | a0001c0002t0001g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(44): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(39): Show |
1 | a0001c0002t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.819-108_819-107ins others(46): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(43): Show |
1 | a0001c0002t0002g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(50): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(45): Show |
1 | a0001c0002t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.819-108_819-107ins others(52): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(43): Show |
1 | a0001c0002t0002g0229 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(50): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(45): Show |
2 | a0001c0002t0001g0172 a0001c0002t0002g0163 |
2 | HG02040.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.819-108_819-107ins others(52): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(47): Show |
1 | a0001c0002t0002g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.819-108_819-107ins others(54): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(45): Show |
1 | a0001c0002t0002g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(52): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(47): Show |
1 | a0001c0002t0002g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.819-108_819-107ins others(54): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(49): Show |
1 | a0001c0002t0002g0164 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(56): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(51): Show |
1 | a0001c0002t0001g0176 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(58): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(49): Show |
1 | a0001c0002t0001g0056 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.819-108_819-107ins others(56): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(51): Show |
1 | a0001c0002t0001g0166 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(58): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146460 | T | TGTGTGTG others(63): Show |
1 | a0001c0002t0002g0171 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.819-108_819-107ins others(70): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146460 | |||||||
| chr10:119146461 | G | A | 18 | a0001c0001t0001g0188 a0001c0001t0001g0221 a0001c0001t0001g0223 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.819-108C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146461 | |||||||
| chr10:119146463 | A | G | 124 | a0001c0001t0001g0188 a0001c0001t0001g0221 a0001c0001t0001g0223 others(121): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.819-110T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146463 | |||||||
| chr10:119146464 | C | CGT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.819-113_819-112dup others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146464 | |||||||
| chr10:119146464 | C | T | 35 | a0001c0001t0001g0188 a0001c0001t0001g0221 a0001c0001t0001g0223 others(32): Show |
35 | HG00408.hp2 HG01361.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.819-111G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146464 | |||||||
| chr10:119146466 | T | C | 1 | a0001c0002t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.819-113A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146466 | |||||||
| chr10:119146476 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.819-123G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146476 | |||||||
| chr10:119146678 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
102 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.819-325G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146678 | |||||||
| chr10:119146804 | G | A | 107 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(104): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.819-451C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146804 | |||||||
| chr10:119146858 | G | A | 2 | a0001c0004t0001g0180 a0001c0004t0001g0181 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.819-505C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119146858 | |||||||
| chr10:119147020 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
103 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.819-667A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147020 | |||||||
| chr10:119147311 | C | T | 1 | a0001c0002t0002g0229 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.818+464G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147311 | |||||||
| chr10:119147380 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0317 others(2): Show |
6 | NA18963.hp1 NA18967.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.818+395C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147380 | |||||||
| chr10:119147476 | C | A | 5 | a0001c0001t0001g0294 a0001c0002t0001g0100 a0001c0002t0001g0115 others(2): Show |
5 | HG01123.hp2 HG01934.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+299G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147476 | |||||||
| chr10:119147494 | C | G | 1 | a0001c0002t0001g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.818+281G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147494 | |||||||
| chr10:119147531 | C | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(359): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.818+244G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147531 | |||||||
| chr10:119147606 | G | A | 90 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.818+169C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147606 | |||||||
| chr10:119147653 | T | A | 1 | a0001c0002t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.818+122A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147653 | |||||||
| chr10:119147661 | T | TG | 50 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0002t0001g0008 others(47): Show |
55 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.818+113dupC | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147661 | |||||||
| chr10:119147691 | C | T | 52 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0002t0001g0008 others(49): Show |
57 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.818+84G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147691 | |||||||
| chr10:119147763 | C | T | 1 | a0001c0001t0002g0305 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.818+12G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 12/13 | chr10 | 119147763 | |||||||
| chr10:119148103 | C | T | 53 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0002t0001g0008 others(50): Show |
58 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.733-243G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148103 | |||||||
| chr10:119148153 | C | T | 3 | a0001c0002t0003g0036 a0001c0002t0003g0037 a0001c0003t0005g0032 |
3 | HG03041.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.733-293G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148153 | |||||||
| chr10:119148154 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.733-294C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148154 | |||||||
| chr10:119148296 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.733-436C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148296 | |||||||
| chr10:119148316 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(105): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.733-456G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148316 | |||||||
| chr10:119148472 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(105): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.733-612A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148472 | |||||||
| chr10:119148473 | G | A | 82 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(79): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.733-613C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148473 | |||||||
| chr10:119148646 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.733-786G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148646 | |||||||
| chr10:119148704 | G | C | 1 | a0001c0002t0001g0025 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.733-844C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148704 | |||||||
| chr10:119148733 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.733-873T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148733 | |||||||
| chr10:119148855 | G | A | 111 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.733-995C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148855 | |||||||
| chr10:119148935 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.733-1075C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148935 | |||||||
| chr10:119148943 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.733-1083C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148943 | |||||||
| chr10:119148955 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.733-1095G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119148955 | |||||||
| chr10:119149089 | G | A | 90 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.733-1229C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149089 | |||||||
| chr10:119149107 | G | A | 1 | a0003c0014t0001g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733-1247C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149107 | |||||||
| chr10:119149127 | T | C | 2 | a0001c0002t0001g0198 a0001c0002t0001g0208 |
2 | NA18951.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.733-1267A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149127 | |||||||
| chr10:119149178 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.733-1318G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149178 | |||||||
| chr10:119149196 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.733-1336G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149196 | |||||||
| chr10:119149241 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.733-1381C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149241 | |||||||
| chr10:119149347 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(359): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.733-1487A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149347 | |||||||
| chr10:119149418 | C | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0209 |
2 | HG00639.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.733-1558G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149418 | |||||||
| chr10:119149503 | A | G | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.733-1643T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149503 | |||||||
| chr10:119149642 | C | T | 1 | a0001c0003t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.733-1782G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149642 | |||||||
| chr10:119149755 | T | G | 1 | a0001c0002t0001g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.733-1895A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149755 | |||||||
| chr10:119149765 | T | G | 110 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(107): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.733-1905A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149765 | |||||||
| chr10:119149801 | T | A | 90 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.733-1941A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149801 | |||||||
| chr10:119149809 | C | T | 5 | a0001c0002t0001g0090 a0001c0002t0002g0027 a0001c0002t0002g0028 others(2): Show |
5 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1949G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149809 | |||||||
| chr10:119149817 | A | C | 1 | a0001c0002t0001g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.733-1957T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149817 | |||||||
| chr10:119149866 | G | A | 1 | a0001c0012t0009g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.733-2006C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149866 | |||||||
| chr10:119149916 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(188): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.733-2056G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149916 | |||||||
| chr10:119149929 | C | T | 111 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.733-2069G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119149929 | |||||||
| chr10:119150059 | G | T | 1 | a0001c0002t0001g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.733-2199C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150059 | |||||||
| chr10:119150116 | C | T | 7 | a0001c0001t0001g0232 a0001c0001t0001g0324 a0001c0001t0001g0325 others(4): Show |
7 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-2256G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150116 | |||||||
| chr10:119150148 | CT | C | 91 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(88): Show |
106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.733-2289delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150148 | |||||||
| chr10:119150198 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.733-2338G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150198 | |||||||
| chr10:119150273 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(103): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.733-2413G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150273 | |||||||
| chr10:119150305 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.733-2445G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150305 | |||||||
| chr10:119150497 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.733-2637G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150497 | |||||||
| chr10:119150517 | C | CT | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.733-2658dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150517 | |||||||
| chr10:119150624 | G | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
102 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.733-2764C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150624 | |||||||
| chr10:119150696 | G | C | 8 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0101 others(5): Show |
8 | HG02135.hp2 HG02148.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-2836C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150696 | |||||||
| chr10:119150799 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0285 a0001c0001t0001g0323 others(2): Show |
5 | HG02074.hp1 NA18954.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2939G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150799 | |||||||
| chr10:119150804 | A | G | 3 | a0001c0004t0001g0180 a0001c0004t0001g0181 a0001c0004t0002g0367 |
3 | HG02280.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.733-2944T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150804 | |||||||
| chr10:119150855 | C | G | 1 | a0001c0002t0001g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.733-2995G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150855 | |||||||
| chr10:119150887 | G | T | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(359): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.733-3027C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150887 | |||||||
| chr10:119150910 | G | A | 50 | a0001c0001t0001g0235 a0001c0001t0001g0250 a0001c0002t0001g0008 others(47): Show |
55 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.733-3050C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150910 | |||||||
| chr10:119150983 | AATCTCAA others(2): Show |
A | 4 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-3132_733-3124d others(11): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119150983 | |||||||
| chr10:119151165 | C | G | 18 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0166 others(15): Show |
18 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.733-3305G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151165 | |||||||
| chr10:119151228 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.733-3368C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151228 | |||||||
| chr10:119151293 | TG | T | 3 | a0001c0001t0001g0286 a0001c0001t0001g0360 a0005c0009t0001g0099 |
3 | NA18957.hp1 NA18981.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.733-3434delC | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151293 | |||||||
| chr10:119151323 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0130 |
3 | HG00735.hp1 HG01891.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.733-3463G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151323 | |||||||
| chr10:119151381 | CA | C | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.733-3522delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151381 | |||||||
| chr10:119151385 | A | C | 2 | a0001c0001t0001g0333 a0001c0003t0001g0033 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.733-3525T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151385 | |||||||
| chr10:119151386 | A | G | 1 | a0001c0002t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.733-3526T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151386 | |||||||
| chr10:119151515 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.732+3547A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151515 | |||||||
| chr10:119151517 | T | A | 1 | a0001c0001t0001g0286 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.732+3545A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151517 | |||||||
| chr10:119151518 | A | T | 1 | a0001c0001t0001g0286 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.732+3544T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151518 | |||||||
| chr10:119151569 | G | A | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.732+3493C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151569 | |||||||
| chr10:119151687 | G | T | 111 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.732+3375C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151687 | |||||||
| chr10:119151738 | A | G | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.732+3324T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151738 | |||||||
| chr10:119151893 | C | T | 54 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0250 others(51): Show |
59 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.732+3169G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151893 | |||||||
| chr10:119151901 | A | G | 1 | a0001c0004t0002g0367 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.732+3161T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119151901 | |||||||
| chr10:119152028 | AGGCTGGT others(7): Show |
A | 1 | a0001c0001t0001g0360 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.732+3020_732+3033d others(16): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152028 | |||||||
| chr10:119152039 | G | A | 18 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0166 others(15): Show |
18 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.732+3023C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152039 | |||||||
| chr10:119152166 | G | T | 20 | a0001c0001t0004g0088 a0001c0002t0001g0056 a0001c0002t0001g0083 others(17): Show |
20 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.732+2896C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152166 | |||||||
| chr10:119152216 | T | A | 1 | a0001c0002t0001g0348 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.732+2846A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152216 | |||||||
| chr10:119152226 | G | A | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.732+2836C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152226 | |||||||
| chr10:119152230 | G | GT | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.732+2831dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152230 | |||||||
| chr10:119152230 | G | GTT | 108 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0178 others(105): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.732+2830_732+2831d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152230 | |||||||
| chr10:119152230 | G | GTTT | 20 | a0001c0001t0004g0088 a0001c0002t0001g0056 a0001c0002t0001g0079 others(17): Show |
20 | HG00673.hp1 HG01433.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.732+2829_732+2831d others(5): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152230 | |||||||
| chr10:119152420 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.732+2642G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152420 | |||||||
| chr10:119152439 | C | G | 3 | a0001c0004t0001g0180 a0001c0004t0001g0181 a0001c0004t0002g0367 |
3 | HG02280.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.732+2623G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152439 | |||||||
| chr10:119152544 | T | C | 4 | a0001c0003t0001g0344 a0001c0003t0001g0364 a0001c0003t0001g0368 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+2518A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152544 | |||||||
| chr10:119152730 | A | ATAGGATT others(14): Show |
2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.732+2311_732+2331d others(23): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152730 | |||||||
| chr10:119152756 | G | A | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.732+2306C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152756 | |||||||
| chr10:119152822 | A | C | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.732+2240T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152822 | |||||||
| chr10:119152913 | A | G | 1 | a0001c0012t0009g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.732+2149T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119152913 | |||||||
| chr10:119153064 | T | C | 90 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.732+1998A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153064 | |||||||
| chr10:119153092 | A | G | 1 | a0001c0004t0002g0367 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.732+1970T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153092 | |||||||
| chr10:119153131 | C | T | 19 | a0001c0001t0002g0331 a0001c0002t0001g0056 a0001c0002t0001g0083 others(16): Show |
19 | HG00408.hp2 HG01361.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.732+1931G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153131 | |||||||
| chr10:119153154 | C | T | 2 | a0001c0001t0004g0088 a0001c0012t0009g0374 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.732+1908G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153154 | |||||||
| chr10:119153351 | T | TAG | 111 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.732+1709_732+1710d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153351 | |||||||
| chr10:119153382 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.732+1680C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153382 | |||||||
| chr10:119153392 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.732+1670C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153392 | |||||||
| chr10:119153402 | C | CA | 7 | a0001c0001t0001g0286 a0001c0002t0001g0100 a0001c0002t0001g0101 others(4): Show |
7 | HG01993.hp2 HG02630.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+1659dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153402 | |||||||
| chr10:119153402 | C | CAA | 85 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(82): Show |
100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.732+1658_732+1659d others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153402 | |||||||
| chr10:119153436 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.732+1626C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153436 | |||||||
| chr10:119153459 | T | C | 2 | a0001c0001t0004g0088 a0001c0012t0009g0374 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.732+1603A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153459 | |||||||
| chr10:119153620 | G | A | 90 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.732+1442C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153620 | |||||||
| chr10:119153662 | T | C | 111 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.732+1400A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153662 | |||||||
| chr10:119153933 | G | A | 2 | a0001c0001t0004g0088 a0001c0012t0009g0374 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.732+1129C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153933 | |||||||
| chr10:119153946 | G | A | 110 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(107): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.732+1116C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153946 | |||||||
| chr10:119153966 | T | G | 1 | a0001c0001t0002g0158 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.732+1096A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153966 | |||||||
| chr10:119153999 | G | A | 4 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+1063C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119153999 | |||||||
| chr10:119154007 | A | C | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.732+1055T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154007 | |||||||
| chr10:119154105 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.732+957C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154105 | |||||||
| chr10:119154106 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.732+956T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154106 | |||||||
| chr10:119154107 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.732+955T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154107 | |||||||
| chr10:119154110 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.732+952C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154110 | |||||||
| chr10:119154177 | CA | C | 11 | a0001c0001t0001g0246 a0001c0001t0001g0277 a0001c0001t0001g0354 others(8): Show |
11 | HG01081.hp2 HG02040.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+884delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154177 | |||||||
| chr10:119154288 | G | C | 2 | a0001c0001t0004g0088 a0001c0012t0009g0374 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.732+774C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154288 | |||||||
| chr10:119154480 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.732+582T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154480 | |||||||
| chr10:119154541 | G | T | 108 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0294 others(105): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.732+521C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154541 | |||||||
| chr10:119154702 | T | C | 4 | a0001c0003t0001g0344 a0001c0003t0001g0364 a0001c0003t0001g0368 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+360A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154702 | |||||||
| chr10:119154801 | C | T | 13 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(10): Show |
15 | HG02004.hp1 HG02523.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.732+261G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154801 | |||||||
| chr10:119154811 | C | T | 9 | a0001c0002t0001g0025 a0001c0002t0001g0085 a0001c0002t0001g0291 others(6): Show |
10 | HG02145.hp2 HG02886.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+251G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154811 | |||||||
| chr10:119154902 | CT | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.732+159delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 11/13 | chr10 | 119154902 | |||||||
| chr10:119155180 | G | A | 91 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(88): Show |
106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.617-3C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155180 | |||||||
| chr10:119155211 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0332 |
2 | HG00323.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.617-34G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155211 | |||||||
| chr10:119155447 | T | A | 1 | a0001c0002t0001g0210 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.617-270A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155447 | |||||||
| chr10:119155478 | T | C | 112 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0001t0002g0331 others(109): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.617-301A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155478 | |||||||
| chr10:119155543 | A | C | 1 | a0001c0001t0001g0311 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.617-366T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155543 | |||||||
| chr10:119155628 | C | G | 111 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.617-451G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155628 | |||||||
| chr10:119155644 | C | G | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.617-467G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155644 | |||||||
| chr10:119155649 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.617-472G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155649 | |||||||
| chr10:119155668 | T | G | 1 | a0001c0002t0001g0118 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.617-491A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155668 | |||||||
| chr10:119155694 | T | C | 92 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(89): Show |
107 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.617-517A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155694 | |||||||
| chr10:119155754 | A | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0048 others(6): Show |
18 | HG01099.hp1 HG01346.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.617-577T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155754 | |||||||
| chr10:119155758 | G | C | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.617-581C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119155758 | |||||||
| chr10:119156020 | T | C | 111 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.616+658A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156020 | |||||||
| chr10:119156024 | T | C | 1 | a0002c0008t0001g0345 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.616+654A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156024 | |||||||
| chr10:119156136 | T | G | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.616+542A>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156136 | |||||||
| chr10:119156143 | C | T | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.616+535G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156143 | |||||||
| chr10:119156151 | G | A | 111 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(108): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.616+527C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156151 | |||||||
| chr10:119156160 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.616+518A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156160 | |||||||
| chr10:119156304 | T | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0342 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+374A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156304 | |||||||
| chr10:119156390 | C | T | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.616+288G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156390 | |||||||
| chr10:119156449 | T | C | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.616+229A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 10/13 | chr10 | 119156449 | |||||||
| chr10:119156807 | G | A | 2 | a0001c0002t0001g0090 a0001c0002t0001g0185 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.538-51C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119156807 | |||||||
| chr10:119156920 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0064 |
3 | HG01069.hp1 HG01071.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.538-164G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119156920 | |||||||
| chr10:119156955 | A | G | 90 | a0001c0001t0001g0242 a0001c0001t0001g0294 a0001c0002t0001g0003 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.538-199T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119156955 | |||||||
| chr10:119157027 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.538-271A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157027 | |||||||
| chr10:119157048 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.538-292G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157048 | |||||||
| chr10:119157208 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0130 |
3 | HG00735.hp1 HG01891.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.538-452G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157208 | |||||||
| chr10:119157323 | C | T | 1 | a0001c0002t0001g0025 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.537+345G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157323 | |||||||
| chr10:119157430 | CA | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.537+237delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157430 | |||||||
| chr10:119157430 | CAA | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0075 others(5): Show |
8 | HG01069.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+236_537+237del others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157430 | |||||||
| chr10:119157433 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.537+235T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157433 | |||||||
| chr10:119157497 | C | G | 1 | a0001c0005t0001g0369 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.537+171G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157497 | |||||||
| chr10:119157532 | A | G | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.537+136T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 9/13 | chr10 | 119157532 | |||||||
| chr10:119157757 | A | T | 364 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(361): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.472-24T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 8/13 | chr10 | 119157757 | |||||||
| chr10:119157933 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
splice_region_variant&intron_variant | LOW | c.415-6C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 7/13 | chr10 | 119157933 | |||||||
| chr10:119157959 | G | A | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.415-32C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 7/13 | chr10 | 119157959 | |||||||
| chr10:119157975 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.414+34T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 7/13 | chr10 | 119157975 | |||||||
| chr10:119158104 | G | A | 89 | a0001c0001t0001g0294 a0001c0002t0001g0003 a0001c0002t0001g0004 others(86): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.361-42C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158104 | |||||||
| chr10:119158158 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.361-96G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158158 | |||||||
| chr10:119158208 | G | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0279 |
3 | NA18951.hp1 NA18995.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.361-146C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158208 | |||||||
| chr10:119158335 | T | A | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.361-273A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158335 | |||||||
| chr10:119158346 | T | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(360): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.361-284A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158346 | |||||||
| chr10:119158398 | A | T | 4 | a0001c0002t0001g0015 a0001c0002t0001g0191 a0001c0002t0001g0195 others(1): Show |
5 | HG00140.hp1 HG00642.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-336T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158398 | |||||||
| chr10:119158472 | C | T | 49 | a0001c0002t0001g0008 a0001c0002t0001g0011 a0001c0002t0001g0015 others(46): Show |
54 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.361-410G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158472 | |||||||
| chr10:119158499 | C | T | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-437G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158499 | |||||||
| chr10:119158615 | C | CA | 90 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0071 others(87): Show |
96 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.361-554dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158615 | |||||||
| chr10:119158615 | CA | C | 19 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
20 | HG01074.hp1 HG01167.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.361-554delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158615 | |||||||
| chr10:119158615 | CAA | C | 9 | a0001c0002t0001g0094 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
9 | HG02257.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.361-555_361-554del others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158615 | |||||||
| chr10:119158615 | CAAA | C | 73 | a0001c0001t0001g0294 a0001c0002t0001g0003 a0001c0002t0001g0004 others(70): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.361-556_361-554del others(3): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158615 | |||||||
| chr10:119158615 | CAAAA | C | 6 | a0001c0002t0001g0053 a0001c0002t0001g0092 a0001c0002t0001g0095 others(3): Show |
6 | HG01070.hp1 HG01257.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-557_361-554del others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158615 | |||||||
| chr10:119158747 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.361-685G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158747 | |||||||
| chr10:119158814 | C | A | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.361-752G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158814 | |||||||
| chr10:119158989 | C | A | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.360+739G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119158989 | |||||||
| chr10:119159031 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360+697C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159031 | |||||||
| chr10:119159237 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.360+491C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159237 | |||||||
| chr10:119159251 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.360+477C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159251 | |||||||
| chr10:119159286 | C | CA | 89 | a0001c0001t0001g0294 a0001c0002t0001g0003 a0001c0002t0001g0004 others(86): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.360+441dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159286 | |||||||
| chr10:119159329 | G | A | 2 | a0001c0002t0001g0090 a0001c0002t0001g0185 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.360+399C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159329 | |||||||
| chr10:119159377 | G | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | NA18953.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.360+351C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159377 | |||||||
| chr10:119159396 | T | C | 2 | a0001c0012t0009g0374 a0003c0014t0001g0373 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.360+332A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159396 | |||||||
| chr10:119159438 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.360+290G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159438 | |||||||
| chr10:119159509 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.360+219C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159509 | |||||||
| chr10:119159537 | TGGGGAG | T | 89 | a0001c0001t0001g0294 a0001c0002t0001g0003 a0001c0002t0001g0004 others(86): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.360+185_360+190del others(6): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159537 | |||||||
| chr10:119159607 | C | T | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360+121G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159607 | |||||||
| chr10:119159667 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.360+61C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 6/13 | chr10 | 119159667 | |||||||
| chr10:119160465 | G | A | 2 | a0001c0002t0001g0083 a0001c0002t0002g0229 |
2 | HG00408.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.334+450C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160465 | |||||||
| chr10:119160474 | C | T | 1 | a0001c0011t0001g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.334+441G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160474 | |||||||
| chr10:119160515 | C | CA | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.334+399dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160515 | |||||||
| chr10:119160515 | C | CAA | 7 | a0001c0001t0001g0279 a0001c0001t0001g0333 a0001c0002t0001g0051 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+398_334+399dup others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160515 | |||||||
| chr10:119160549 | G | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+366C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160549 | |||||||
| chr10:119160550 | G | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+365C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160550 | |||||||
| chr10:119160551 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+364T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160551 | |||||||
| chr10:119160553 | A | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+362T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160553 | |||||||
| chr10:119160554 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+361T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160554 | |||||||
| chr10:119160555 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+360T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160555 | |||||||
| chr10:119160562 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+353T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160562 | |||||||
| chr10:119160563 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+352T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160563 | |||||||
| chr10:119160564 | G | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+351C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160564 | |||||||
| chr10:119160565 | C | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+350G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160565 | |||||||
| chr10:119160566 | A | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+349T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160566 | |||||||
| chr10:119160567 | A | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+348T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160567 | |||||||
| chr10:119160568 | G | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+347C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160568 | |||||||
| chr10:119160569 | G | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+346C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160569 | |||||||
| chr10:119160588 | C | CT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0178 a0001c0001t0001g0190 others(10): Show |
13 | HG00621.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+326dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160588 | |||||||
| chr10:119160588 | CT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(112): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.334+326delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160588 | |||||||
| chr10:119160588 | CTT | C | 101 | a0001c0001t0002g0158 a0001c0002t0001g0003 a0001c0002t0001g0004 others(98): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.334+325_334+326del others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160588 | |||||||
| chr10:119160590 | T | C | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+325A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160590 | |||||||
| chr10:119160593 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.334+322A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160593 | |||||||
| chr10:119160612 | G | A | 88 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0007 others(85): Show |
103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.334+303C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160612 | |||||||
| chr10:119160619 | C | A | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+296G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160619 | |||||||
| chr10:119160620 | A | G | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+295T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160620 | |||||||
| chr10:119160627 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.334+288A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160627 | |||||||
| chr10:119160659 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+256T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160659 | |||||||
| chr10:119160700 | A | T | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+215T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160700 | |||||||
| chr10:119160726 | A | G | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+189T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160726 | |||||||
| chr10:119160761 | A | G | 1 | a0001c0002t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+154T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160761 | |||||||
| chr10:119160820 | G | A | 2 | a0001c0002t0001g0321 a0001c0002t0001g0349 |
2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.334+95C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 5/13 | chr10 | 119160820 | |||||||
| chr10:119160985 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.280-16A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 4/13 | chr10 | 119160985 | |||||||
| chr10:119161117 | T | A | 1 | a0001c0001t0001g0343 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.253-36A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161117 | |||||||
| chr10:119161378 | T | A | 90 | a0001c0001t0001g0077 a0001c0001t0001g0343 a0001c0002t0001g0003 others(87): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.253-297A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161378 | |||||||
| chr10:119161412 | A | C | 1 | a0001c0002t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.253-331T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161412 | |||||||
| chr10:119161427 | C | A | 156 | a0001c0001t0001g0077 a0001c0001t0001g0343 a0001c0002t0001g0003 others(153): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.253-346G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161427 | |||||||
| chr10:119161430 | A | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | NA18946.hp2 NA18952.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-349T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161430 | |||||||
| chr10:119161436 | A | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.253-355T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161436 | |||||||
| chr10:119161437 | C | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0126 a0001c0002t0001g0150 others(1): Show |
4 | HG01192.hp1 HG02074.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-356G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161437 | |||||||
| chr10:119161437 | C | CA | 25 | a0001c0001t0001g0084 a0001c0001t0001g0146 a0001c0001t0001g0334 others(22): Show |
26 | HG01934.hp1 HG02145.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.253-357dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161437 | |||||||
| chr10:119161437 | C | CCAA | 80 | a0001c0001t0001g0077 a0001c0001t0001g0343 a0001c0002t0001g0003 others(77): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.253-357_253-356ins others(3): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161437 | |||||||
| chr10:119161437 | C | CCAAA | 5 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(2): Show |
5 | HG00741.hp1 HG01123.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-357_253-356ins others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161437 | |||||||
| chr10:119161512 | A | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(360): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.253-431T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161512 | |||||||
| chr10:119161569 | A | G | 2 | a0001c0004t0001g0180 a0001c0004t0001g0181 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.253-488T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161569 | |||||||
| chr10:119161641 | G | T | 2 | a0001c0003t0001g0344 a0001c0003t0001g0364 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.253-560C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161641 | |||||||
| chr10:119161761 | G | A | 2 | a0001c0002t0001g0090 a0001c0002t0001g0185 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.252+579C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161761 | |||||||
| chr10:119161779 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.252+561C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161779 | |||||||
| chr10:119161886 | G | A | 371 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(368): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.252+454C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161886 | |||||||
| chr10:119161966 | C | G | 1 | a0001c0001t0002g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.252+374G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119161966 | |||||||
| chr10:119162111 | G | T | 20 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(17): Show |
20 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.252+229C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119162111 | |||||||
| chr10:119162249 | A | G | 4 | a0001c0002t0003g0036 a0001c0002t0003g0037 a0001c0012t0009g0374 others(1): Show |
4 | HG02559.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+91T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 3/13 | chr10 | 119162249 | |||||||
| chr10:119162505 | T | C | 89 | a0001c0001t0001g0077 a0001c0001t0001g0221 a0001c0001t0001g0343 others(86): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.178-91A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162505 | |||||||
| chr10:119162563 | T | C | 25 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(22): Show |
32 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.178-149A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162563 | |||||||
| chr10:119162633 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0231 |
3 | HG02683.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.178-219G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162633 | |||||||
| chr10:119162655 | C | G | 2 | a0001c0002t0001g0090 a0001c0002t0001g0185 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.178-241G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162655 | |||||||
| chr10:119162758 | T | C | 1 | a0001c0005t0001g0372 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.178-344A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162758 | |||||||
| chr10:119162775 | CCT | C | 87 | a0001c0001t0001g0221 a0001c0002t0001g0003 a0001c0002t0001g0004 others(84): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.178-363_178-362del others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162775 | |||||||
| chr10:119162792 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(107): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.178-378A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162792 | |||||||
| chr10:119162864 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.178-450A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119162864 | |||||||
| chr10:119163168 | C | T | 1 | a0001c0012t0009g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178-754G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163168 | |||||||
| chr10:119163227 | TTTC | T | 19 | a0001c0002t0001g0056 a0001c0002t0001g0083 a0001c0002t0001g0162 others(16): Show |
19 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-816_178-814del others(3): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163227 | |||||||
| chr10:119163233 | C | CT | 25 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
28 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.178-820dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163233 | |||||||
| chr10:119163233 | CT | C | 101 | a0001c0001t0001g0077 a0001c0001t0001g0143 a0001c0001t0001g0146 others(98): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.178-820delA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163233 | |||||||
| chr10:119163315 | A | G | 8 | a0001c0002t0001g0335 a0001c0002t0002g0027 a0001c0002t0002g0028 others(5): Show |
8 | HG02280.hp1 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+816T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163315 | |||||||
| chr10:119163388 | C | T | 18 | a0001c0002t0001g0083 a0001c0002t0001g0162 a0001c0002t0001g0166 others(15): Show |
18 | HG00408.hp2 HG01074.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+743G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163388 | |||||||
| chr10:119163526 | C | G | 3 | a0001c0002t0002g0293 a0001c0002t0003g0036 a0001c0002t0003g0037 |
3 | HG03041.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.177+605G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163526 | |||||||
| chr10:119163593 | C | G | 131 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.177+538G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163593 | |||||||
| chr10:119163655 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
6 | HG02083.hp2 NA18966.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+476C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163655 | |||||||
| chr10:119163827 | G | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(177): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.177+304C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163827 | |||||||
| chr10:119163988 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.177+143G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119163988 | |||||||
| chr10:119164040 | C | CA | 26 | a0001c0001t0001g0035 a0001c0001t0001g0145 a0001c0001t0001g0146 others(23): Show |
27 | HG00741.hp1 HG01175.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+90dupT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119164040 | |||||||
| chr10:119164040 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(91): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.177+90delT | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 2/13 | chr10 | 119164040 | |||||||
| chr10:119164268 | C | CT | 122 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.112-73dupA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164268 | |||||||
| chr10:119164268 | C | CTT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(174): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.112-74_112-73dupAA | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164268 | |||||||
| chr10:119164268 | C | CTTT | 21 | a0001c0001t0001g0031 a0001c0001t0001g0217 a0001c0001t0001g0218 others(18): Show |
21 | HG00423.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.112-75_112-73dupAA others(1): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164268 | |||||||
| chr10:119164268 | C | CTTTT | 44 | a0001c0001t0001g0014 a0001c0001t0001g0184 a0001c0001t0001g0188 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.112-76_112-73dupAA others(2): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164268 | |||||||
| chr10:119164482 | A | G | 1 | a0001c0002t0001g0042 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.112-286T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164482 | |||||||
| chr10:119164528 | T | C | 5 | a0001c0005t0001g0369 a0001c0005t0001g0370 a0001c0005t0001g0372 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-332A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164528 | |||||||
| chr10:119164530 | C | T | 19 | a0001c0001t0001g0178 a0001c0001t0008g0179 a0001c0002t0001g0162 others(16): Show |
19 | HG00438.hp1 HG00621.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.112-334G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164530 | |||||||
| chr10:119164635 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.112-439G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164635 | |||||||
| chr10:119164752 | C | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(366): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.112-556G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164752 | |||||||
| chr10:119164753 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.112-557G>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164753 | |||||||
| chr10:119164780 | A | C | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-584T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164780 | |||||||
| chr10:119164781 | A | C | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-585T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164781 | |||||||
| chr10:119164782 | A | C | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-586T>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164782 | |||||||
| chr10:119164785 | A | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-589T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164785 | |||||||
| chr10:119164791 | G | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-595C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164791 | |||||||
| chr10:119164793 | A | G | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-597T>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164793 | |||||||
| chr10:119164794 | C | A | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-598G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164794 | |||||||
| chr10:119164802 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.112-606A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164802 | |||||||
| chr10:119164804 | G | A | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-608C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164804 | |||||||
| chr10:119164806 | A | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-610T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164806 | |||||||
| chr10:119164813 | T | A | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-617A>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164813 | |||||||
| chr10:119164817 | A | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-621T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164817 | |||||||
| chr10:119164820 | G | C | 2 | a0001c0003t0001g0364 a0001c0003t0003g0363 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.112-624C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164820 | |||||||
| chr10:119164822 | A | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-626T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164822 | |||||||
| chr10:119164823 | C | A | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-627G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164823 | |||||||
| chr10:119164829 | A | T | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-633T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164829 | |||||||
| chr10:119164835 | C | A | 1 | a0001c0002t0001g0365 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.112-639G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164835 | |||||||
| chr10:119164849 | G | A | 3 | a0001c0002t0001g0155 a0001c0002t0001g0156 a0001c0002t0001g0157 |
3 | HG01346.hp2 HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.112-653C>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164849 | |||||||
| chr10:119164857 | C | A | 3 | a0001c0002t0002g0366 a0001c0003t0001g0368 a0001c0004t0002g0367 |
3 | HG02257.hp2 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.112-661G>T | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164857 | |||||||
| chr10:119164878 | T | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(367): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.111+659A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119164878 | |||||||
| chr10:119165000 | T | C | 3 | a0001c0001t0001g0031 a0001c0003t0001g0033 a0001c0003t0005g0032 |
3 | HG02258.hp1 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.111+537A>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165000 | |||||||
| chr10:119165023 | C | CTGTT | 370 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(367): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.111+510_111+513dup others(4): Show |
SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165023 | |||||||
| chr10:119165139 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.111+398T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165139 | |||||||
| chr10:119165176 | G | T | 1 | a0001c0002t0001g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.111+361C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165176 | |||||||
| chr10:119165351 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0002g0039 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.111+186G>C | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165351 | |||||||
| chr10:119165362 | G | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(367): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.111+175C>G | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165362 | |||||||
| chr10:119165415 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.111+122C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165415 | |||||||
| chr10:119165418 | G | T | 7 | a0001c0001t0001g0031 a0001c0002t0002g0027 a0001c0002t0002g0028 others(4): Show |
7 | HG02258.hp1 HG02630.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+119C>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165418 | |||||||
| chr10:119165419 | A | T | 7 | a0001c0001t0001g0031 a0001c0002t0002g0027 a0001c0002t0002g0028 others(4): Show |
7 | HG02258.hp1 HG02630.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+118T>A | SFXN4 | ENSG00000183605.17 | transcript | ENST00000355697.7 | protein_coding | 1/13 | chr10 | 119165419 |