Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22824 |
| ensemblid | ENSG00000164070.12 |
| hgncid | 17041 |
| symbol | HSPA4L |
| name | heat shock protein family A (Hsp70) member 4 like |
| refseq_nuc | NM_014278.4 |
| refseq_prot | NP_055093.2 |
| ensembl_nuc | ENST00000296464.9 |
| ensembl_prot | ENSP00000296464.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 127782322 |
| end | 127840733 |
| strand | + |
| ver | v1.2 |
| region | chr4:127782322-127840733 |
| region5000 | chr4:127777322-127845733 |
| regionname0 | HSPA4L_chr4_127782322_127840733 |
| regionname5000 | HSPA4L_chr4_127777322_127845733 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 839 | 236 | 70 | 31 | 117 | 4 | 14 | 87 | HSPA4L_chr4_127777322_127845733 | HSPA4L | MSVVG others(834): Show |
chr4 | 127777322 | 127845733 |
| a0002 | 1/0 | 839 | 97 | 16 | 15 | 51 | 5 | 9 | 43 | HSPA4L_chr4_127777322_127845733 | HSPA4L | MSVVG others(834): Show |
chr4 | 127777322 | 127845733 |
| a0003 | 0/1 | 839 | 6 | 0 | 4 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | MSVVG others(834): Show |
chr4 | 127777322 | 127845733 |
| a0004 | 0/0 | 839 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | MSVVG others(834): Show |
chr4 | 127777322 | 127845733 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2517 | 213 | 49 | 30 | 116 | 4 | 14 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0001c0003 | 0/0 | 2517 | 15 | 14 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0001c0005 | 0/0 | 2517 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0001c0006 | 0/0 | 2517 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0001c0008 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0002c0002 | 1/0 | 2517 | 93 | 15 | 13 | 50 | 5 | 9 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0002c0007 | 0/0 | 2517 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0002c0010 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0002c0011 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0003c0004 | 0/1 | 2517 | 6 | 0 | 4 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 | ||
| a0004c0009 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | ATGTC others(2512): Show |
chr4 | 127777322 | 127845733 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10608 | 91 | 13 | 15 | 48 | 4 | 11 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0002 | 0/0 | 10608 | 57 | 0 | 7 | 50 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0004 | 0/0 | 10609 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0005 | 0/0 | 10608 | 8 | 8 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0008 | 0/0 | 10611 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10606): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0009 | 0/0 | 10613 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10608): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0010 | 0/0 | 10607 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10602): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0012 | 0/0 | 10608 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0013 | 0/0 | 10608 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0014 | 0/0 | 10608 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0015 | 0/0 | 10608 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0016 | 0/0 | 10608 | 3 | 0 | 3 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0017 | 0/0 | 10608 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0018 | 0/0 | 10611 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10606): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0021 | 0/0 | 10608 | 2 | 0 | 0 | 0 | 0 | 2 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0022 | 0/0 | 10607 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10602): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0024 | 0/0 | 10608 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0025 | 0/0 | 10609 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0026 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0027 | 0/0 | 10629 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10624): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0029 | 0/0 | 10608 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0031 | 0/0 | 10612 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10607): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0033 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0035 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0036 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0040 | 0/0 | 10608 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0042 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0043 | 0/0 | 10637 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10632): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0045 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0047 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0048 | 0/0 | 10606 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10601): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0049 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0051 | 0/0 | 10607 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10602): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0052 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0053 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0054 | 0/0 | 10627 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10622): Show |
chr4 | 127777322 | 127845733 |
| a0001c0001t0055 | 0/0 | 10646 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10641): Show |
chr4 | 127777322 | 127845733 |
| a0001c0003t0001 | 0/0 | 10608 | 15 | 14 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0005t0007 | 0/0 | 10615 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10610): Show |
chr4 | 127777322 | 127845733 |
| a0001c0006t0011 | 0/0 | 10608 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0001c0008t0044 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0001 | 1/0 | 10608 | 51 | 12 | 9 | 16 | 5 | 8 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0003 | 0/0 | 10609 | 12 | 0 | 0 | 12 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0004 | 0/0 | 10609 | 8 | 0 | 0 | 8 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0006 | 0/0 | 10609 | 5 | 0 | 0 | 4 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0009 | 0/0 | 10613 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10608): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0019 | 0/0 | 10609 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0023 | 0/0 | 10608 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0028 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0032 | 0/0 | 10608 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0034 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0037 | 0/0 | 10610 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10605): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0038 | 0/0 | 10609 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0039 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0046 | 0/0 | 10608 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0050 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0056 | 0/0 | 10610 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10605): Show |
chr4 | 127777322 | 127845733 |
| a0002c0002t0057 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0007t0001 | 0/0 | 10608 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0010t0001 | 0/0 | 10608 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0002c0011t0001 | 0/0 | 10608 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0003c0004t0001 | 0/0 | 10608 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0003c0004t0020 | 0/0 | 10608 | 2 | 0 | 1 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0003c0004t0030 | 0/0 | 10608 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| a0003c0004t0041 | 0/1 | 10609 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10604): Show |
chr4 | 127777322 | 127845733 |
| a0004c0009t0001 | 0/0 | 10608 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | AGTAG others(10603): Show |
chr4 | 127777322 | 127845733 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 2 | 2 | 4 | 1 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0010g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0013g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0014g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0015g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0016g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0016g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0018g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0021g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0021g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0022g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0024g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0024g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0025g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0026g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0027g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0029g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0033g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0035g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0036g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0040g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0042g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0043g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0045g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0047g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0048g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0049g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0051g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0052g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0053g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0054g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0001t0055g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0005t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0005t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0005t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0005t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0006t0011g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0006t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0001c0008t0044g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0002 | 0/0 | 7 | 0 | 3 | 1 | 0 | 3 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0004g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0006g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0009g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0009g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0019g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0019g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0023g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0023g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0032g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0037g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0038g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0039g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0046g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0050g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0056g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0002t0057g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0007t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0007t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0010t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0002c0011t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0020g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0020g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0030g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0003c0004t0041g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| a0004c0009t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0168 | EUR | GBR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00099 | hp2 | a0003 | c0004 | t0020 | g0075 | EUR | GBR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0191 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00558 | hp1 | a0001 | c0001 | t0022 | g0207 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00597 | hp1 | a0002 | c0002 | t0039 | g0117 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG00741 | hp2 | a0002 | c0002 | t0046 | g0170 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01070 | hp1 | a0002 | c0007 | t0001 | g0128 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01106 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01106 | hp2 | a0002 | c0007 | t0001 | g0002 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01109 | hp2 | a0001 | c0001 | t0015 | g0041 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0189 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01175 | hp1 | a0002 | c0002 | t0023 | g0002 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01192 | hp2 | a0003 | c0004 | t0030 | g0024 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01256 | hp2 | a0003 | c0004 | t0001 | g0024 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01258 | hp1 | a0001 | c0001 | t0029 | g0096 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01346 | hp1 | a0002 | c0002 | t0023 | g0112 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01358 | hp1 | a0003 | c0004 | t0020 | g0076 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01433 | hp2 | a0001 | c0001 | t0016 | g0005 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0039 | AMR | CLM | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0126 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0120 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0121 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01891 | hp1 | a0001 | c0001 | t0049 | g0001 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01891 | hp2 | a0001 | c0005 | t0007 | g0181 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01981 | hp1 | a0002 | c0002 | t0032 | g0115 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02004 | hp2 | a0001 | c0001 | t0043 | g0031 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02015 | hp2 | a0002 | c0002 | t0038 | g0131 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02027 | hp2 | a0002 | c0011 | t0001 | g0002 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02055 | hp1 | a0001 | c0006 | t0011 | g0040 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02080 | hp2 | a0002 | c0002 | t0004 | g0147 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02145 | hp2 | a0001 | c0001 | t0031 | g0018 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02155 | hp1 | a0001 | c0001 | t0035 | g0023 | EAS | CDX | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0093 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02273 | hp1 | a0001 | c0001 | t0016 | g0055 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02280 | hp1 | a0001 | c0001 | t0054 | g0190 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0152 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02300 | hp1 | a0001 | c0001 | t0016 | g0005 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0153 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02451 | hp2 | a0001 | c0001 | t0018 | g0018 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0154 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02602 | hp1 | a0004 | c0009 | t0001 | g0002 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02615 | hp1 | a0002 | c0010 | t0001 | g0172 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02622 | hp1 | a0001 | c0005 | t0007 | g0183 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02630 | hp2 | a0001 | c0001 | t0045 | g0091 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02809 | hp1 | a0001 | c0001 | t0025 | g0037 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02897 | hp1 | a0002 | c0002 | t0050 | g0107 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0041 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0039 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02965 | hp1 | a0001 | c0001 | t0036 | g0157 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0188 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02976 | hp2 | a0001 | c0006 | t0011 | g0040 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03041 | hp1 | a0002 | c0002 | t0028 | g0012 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0108 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03195 | hp2 | a0001 | c0001 | t0053 | g0156 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03209 | hp2 | a0001 | c0006 | t0011 | g0155 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03225 | hp2 | a0001 | c0005 | t0007 | g0182 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0001 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03486 | hp1 | a0001 | c0001 | t0042 | g0162 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0187 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0082 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03579 | hp2 | a0001 | c0001 | t0018 | g0018 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | BEB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04184 | hp1 | a0001 | c0001 | t0021 | g0080 | SAS | BEB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04199 | hp1 | a0002 | c0002 | t0006 | g0110 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04204 | hp2 | a0001 | c0001 | t0040 | g0097 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04228 | hp1 | a0001 | c0001 | t0021 | g0029 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0225 | EAS | CHB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18747 | hp2 | a0001 | c0008 | t0044 | g0062 | EAS | CHB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18906 | hp1 | a0001 | c0001 | t0026 | g0144 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18941 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18946 | hp2 | a0001 | c0001 | t0022 | g0209 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18947 | hp1 | a0001 | c0001 | t0014 | g0226 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18948 | hp2 | a0002 | c0002 | t0019 | g0114 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18949 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18952 | hp2 | a0002 | c0002 | t0003 | g0034 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18954 | hp1 | a0002 | c0002 | t0057 | g0010 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18957 | hp2 | a0002 | c0002 | t0056 | g0010 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18959 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18959 | hp2 | a0001 | c0001 | t0047 | g0001 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18960 | hp2 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18961 | hp1 | a0001 | c0001 | t0014 | g0224 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18961 | hp2 | a0002 | c0002 | t0019 | g0032 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18966 | hp2 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18968 | hp1 | a0002 | c0002 | t0009 | g0123 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0148 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18978 | hp2 | a0002 | c0002 | t0004 | g0150 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18981 | hp1 | a0002 | c0002 | t0034 | g0002 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0038 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0116 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19001 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19001 | hp2 | a0001 | c0001 | t0051 | g0197 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19002 | hp1 | a0001 | c0001 | t0033 | g0214 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19009 | hp1 | a0001 | c0001 | t0010 | g0049 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19009 | hp2 | a0002 | c0002 | t0009 | g0033 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19011 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0034 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19070 | hp2 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19072 | hp1 | a0002 | c0002 | t0009 | g0033 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19072 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19075 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19076 | hp1 | a0002 | c0002 | t0003 | g0132 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19077 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19086 | hp2 | a0001 | c0001 | t0010 | g0049 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19240 | hp1 | a0001 | c0001 | t0015 | g0161 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA19240 | hp2 | a0001 | c0001 | t0055 | g0164 | AFR | YRI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ASW | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | TSI | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02486 | hp1 | a0001 | c0001 | t0052 | g0185 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02486 | hp2 | a0001 | c0005 | t0007 | g0184 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02559 | hp1 | a0002 | c0002 | t0037 | g0149 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | MSL | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | USA | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18955 | hp1 | a0001 | c0001 | t0048 | g0208 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | LWK | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | LWK | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0041 | g0074 | REF | REF | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0169 | REF | REF | HSPA4L_chr4_127777322_127845733 | HSPA4L | chr4 | 127777322 | 127845733 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127801887 | T | C | 2 | a0001 a0003 |
241 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(238): Show |
missense_variant | MODERATE | c.632T>C | p.Leu211Ser | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/19 | 861/10608 | 632/2520 | 211/839 | chr4 | 127801887 | |||
| chr4:127811506 | G | A | 1 | a0004 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1448G>A | p.Arg483His | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/19 | 1677/10608 | 1448/2520 | 483/839 | chr4 | 127811506 | |||
| chr4:127820555 | T | C | 1 | a0003 | 5 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(2): Show |
missense_variant | MODERATE | c.1802T>C | p.Ile601Thr | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/19 | 2031/10608 | 1802/2520 | 601/839 | chr4 | 127820555 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127795779 | C | T | 1 | a0001c0005 | 4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.177C>T | p.Asn59Asn | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/19 | 406/10608 | 177/2520 | 59/839 | chr4 | 127795779 | |||
| chr4:127803793 | A | T | 1 | a0002c0011 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.828A>T | p.Leu276Leu | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 7/19 | 1057/10608 | 828/2520 | 276/839 | chr4 | 127803793 | |||
| chr4:127808083 | A | G | 1 | a0001c0006 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1332A>G | p.Ala444Ala | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/19 | 1561/10608 | 1332/2520 | 444/839 | chr4 | 127808083 | |||
| chr4:127823573 | C | T | 1 | a0001c0008 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.1995C>T | p.Asp665Asp | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/19 | 2224/10608 | 1995/2520 | 665/839 | chr4 | 127823573 | |||
| chr4:127827310 | C | T | 1 | a0002c0007 | 2 | HG01070.hp1 HG01106.hp2 |
synonymous_variant | LOW | c.2052C>T | p.Tyr684Tyr | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/19 | 2281/10608 | 2052/2520 | 684/839 | chr4 | 127827310 | |||
| chr4:127830649 | T | C | 2 | a0001c0003 a0002c0010 |
16 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
synonymous_variant | LOW | c.2178T>C | p.Tyr726Tyr | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/19 | 2407/10608 | 2178/2520 | 726/839 | chr4 | 127830649 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127782335 | C | CCAGGCTG others(12): Show |
1 | a0001c0001t0054 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205_-187dupGACGCG others(13): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | 186 | INFO_REALIGN_3_PRIME | chr4 | 127782335 | |||||
| chr4:127782335 | C | CCAGGCTG others(31): Show |
1 | a0001c0001t0055 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187_-186insGACGCG others(32): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | 186 | INFO_REALIGN_3_PRIME | chr4 | 127782335 | |||||
| chr4:127782356 | A | G | 2 | a0002c0002t0056 a0002c0002t0057 |
2 | NA18954.hp1 NA18957.hp2 |
5_prime_UTR_variant | MODIFIER | c.-195A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | 195 | chr4 | 127782356 | ||||||
| chr4:127782377 | C | G | 1 | a0001c0001t0053 | 1 | HG03195.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-174C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | chr4 | 127782377 | |||||||
| chr4:127782426 | C | T | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-125C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | 125 | chr4 | 127782426 | ||||||
| chr4:127782511 | G | A | 6 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0025 others(3): Show |
16 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/19 | 40 | chr4 | 127782511 | ||||||
| chr4:127833070 | C | T | 1 | a0001c0001t0051 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 196 | chr4 | 127833070 | ||||||
| chr4:127833103 | G | A | 1 | a0002c0002t0028 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*229G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 229 | chr4 | 127833103 | ||||||
| chr4:127833190 | A | G | 1 | a0001c0001t0024 | 2 | HG03130.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*316A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 316 | chr4 | 127833190 | ||||||
| chr4:127833524 | G | A | 1 | a0001c0001t0029 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 650 | chr4 | 127833524 | ||||||
| chr4:127833702 | G | A | 2 | a0001c0001t0012 a0001c0001t0013 |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 828 | chr4 | 127833702 | ||||||
| chr4:127833903 | G | A | 1 | a0003c0004t0030 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1029 | chr4 | 127833903 | ||||||
| chr4:127834201 | AG | A | 3 | a0001c0001t0018 a0001c0001t0031 a0001c0005t0007 |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1328delG | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1328 | chr4 | 127834201 | ||||||
| chr4:127834478 | C | T | 1 | a0002c0002t0050 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1604C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1604 | chr4 | 127834478 | ||||||
| chr4:127834493 | A | C | 1 | a0002c0002t0023 | 2 | HG01175.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1619A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1619 | chr4 | 127834493 | ||||||
| chr4:127834588 | T | C | 1 | a0002c0002t0032 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1714T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1714 | chr4 | 127834588 | ||||||
| chr4:127834657 | G | A | 1 | a0001c0001t0014 | 3 | NA18747.hp1 NA18947.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1783 | chr4 | 127834657 | ||||||
| chr4:127834723 | C | A | 3 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0026 |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1849C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1849 | chr4 | 127834723 | ||||||
| chr4:127834805 | G | A | 1 | a0001c0001t0033 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 1931 | chr4 | 127834805 | ||||||
| chr4:127834894 | T | TAGTC | 1 | a0001c0005t0007 | 4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2023_*2026dupTCAG | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2027 | INFO_REALIGN_3_PRIME | chr4 | 127834894 | |||||
| chr4:127835096 | A | C | 1 | a0001c0001t0049 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2222A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2222 | chr4 | 127835096 | ||||||
| chr4:127835201 | CAG | C | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(4): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2328_*2329delAG | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2328 | chr4 | 127835201 | ||||||
| chr4:127835372 | G | A | 1 | a0001c0006t0011 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2498G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2498 | chr4 | 127835372 | ||||||
| chr4:127835376 | G | T | 1 | a0001c0001t0021 | 2 | HG04184.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2502G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2502 | chr4 | 127835376 | ||||||
| chr4:127835618 | G | A | 1 | a0002c0002t0034 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2744G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2744 | chr4 | 127835618 | ||||||
| chr4:127835657 | C | T | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2783C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2783 | chr4 | 127835657 | ||||||
| chr4:127835658 | G | A | 1 | a0001c0001t0035 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2784G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2784 | chr4 | 127835658 | ||||||
| chr4:127835698 | G | A | 1 | a0001c0001t0036 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2824 | chr4 | 127835698 | ||||||
| chr4:127835702 | C | CA | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(5): Show |
76 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2838dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2839 | INFO_REALIGN_3_PRIME | chr4 | 127835702 | |||||
| chr4:127835815 | G | GACTC | 3 | a0001c0001t0018 a0001c0001t0031 a0001c0005t0007 |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2944_*2947dupTCAC | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2948 | INFO_REALIGN_3_PRIME | chr4 | 127835815 | |||||
| chr4:127835824 | C | T | 3 | a0001c0001t0018 a0001c0001t0031 a0001c0005t0007 |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2950C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 2950 | chr4 | 127835824 | ||||||
| chr4:127835910 | C | T | 1 | a0001c0001t0047 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3036C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3036 | chr4 | 127835910 | ||||||
| chr4:127836117 | C | T | 1 | a0002c0002t0046 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3243C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3243 | chr4 | 127836117 | ||||||
| chr4:127836164 | A | G | 1 | a0003c0004t0020 | 2 | HG00099.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3290A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3290 | chr4 | 127836164 | ||||||
| chr4:127836228 | A | G | 1 | a0001c0001t0045 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3354A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3354 | chr4 | 127836228 | ||||||
| chr4:127836240 | G | A | 1 | a0001c0001t0045 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3366G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3366 | chr4 | 127836240 | ||||||
| chr4:127836346 | A | G | 1 | a0001c0001t0026 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3472A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3472 | chr4 | 127836346 | ||||||
| chr4:127836367 | A | AAAAAC | 2 | a0001c0001t0009 a0002c0002t0009 |
4 | NA18968.hp1 NA19009.hp2 NA19072.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3508_*3512dupCAAA others(1): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3513 | INFO_REALIGN_3_PRIME | chr4 | 127836367 | |||||
| chr4:127836371 | A | T | 1 | a0001c0008t0044 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3497A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3497 | chr4 | 127836371 | ||||||
| chr4:127836457 | T | TG | 13 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(10): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3592dupG | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 3593 | INFO_REALIGN_3_PRIME | chr4 | 127836457 | |||||
| chr4:127837017 | T | G | 1 | a0002c0002t0046 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4143T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4143 | chr4 | 127837017 | ||||||
| chr4:127837628 | T | TTTAATCT others(14): Show |
1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4766_*4767insCCAC others(17): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4767 | INFO_REALIGN_3_PRIME | chr4 | 127837628 | |||||
| chr4:127837662 | G | T | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4788G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4788 | chr4 | 127837662 | ||||||
| chr4:127837704 | T | A | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4830T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4830 | chr4 | 127837704 | ||||||
| chr4:127837705 | G | C | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4831G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4831 | chr4 | 127837705 | ||||||
| chr4:127837732 | A | T | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4858 | chr4 | 127837732 | ||||||
| chr4:127837747 | A | T | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4873A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4873 | chr4 | 127837747 | ||||||
| chr4:127837757 | T | A | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4883T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4883 | chr4 | 127837757 | ||||||
| chr4:127837758 | G | C | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4884G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4884 | chr4 | 127837758 | ||||||
| chr4:127837776 | T | A | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4902T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4902 | chr4 | 127837776 | ||||||
| chr4:127837781 | T | A | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4907T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4907 | chr4 | 127837781 | ||||||
| chr4:127837791 | G | C | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4917G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4917 | chr4 | 127837791 | ||||||
| chr4:127837812 | G | GT | 4 | a0001c0001t0018 a0001c0001t0031 a0001c0005t0007 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4948dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4949 | INFO_REALIGN_3_PRIME | chr4 | 127837812 | |||||
| chr4:127837814 | T | C | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4940T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4940 | chr4 | 127837814 | ||||||
| chr4:127837815 | T | A | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4941T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4941 | chr4 | 127837815 | ||||||
| chr4:127837816 | T | C | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4942T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4942 | chr4 | 127837816 | ||||||
| chr4:127837817 | T | G | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4943T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4943 | chr4 | 127837817 | ||||||
| chr4:127837818 | T | C | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4944T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 4944 | chr4 | 127837818 | ||||||
| chr4:127837973 | T | TTTTGTAT others(22): Show |
1 | a0001c0001t0043 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5100_*5128dupTTTG others(25): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5129 | INFO_REALIGN_3_PRIME | chr4 | 127837973 | |||||
| chr4:127838104 | A | G | 1 | a0001c0001t0013 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5230A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5230 | chr4 | 127838104 | ||||||
| chr4:127838168 | C | G | 1 | a0001c0001t0042 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5294C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5294 | chr4 | 127838168 | ||||||
| chr4:127838181 | T | C | 1 | a0002c0002t0019 | 2 | NA18948.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5307T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5307 | chr4 | 127838181 | ||||||
| chr4:127838449 | T | C | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(14): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*5575T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5575 | chr4 | 127838449 | ||||||
| chr4:127838651 | T | C | 3 | a0002c0002t0003 a0002c0002t0019 a0002c0002t0039 |
15 | HG00597.hp1 HG02083.hp1 NA18948.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5777T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5777 | chr4 | 127838651 | ||||||
| chr4:127838674 | A | G | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5800A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 5800 | chr4 | 127838674 | ||||||
| chr4:127838926 | T | C | 1 | a0001c0001t0040 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6052T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6052 | chr4 | 127838926 | ||||||
| chr4:127838941 | G | GTTA | 1 | a0001c0001t0008 | 4 | HG02257.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6070_*6072dupATT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6073 | INFO_REALIGN_3_PRIME | chr4 | 127838941 | |||||
| chr4:127838954 | G | A | 2 | a0001c0001t0015 a0001c0001t0042 |
4 | HG01109.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6080G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6080 | chr4 | 127838954 | ||||||
| chr4:127838963 | T | C | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(4): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*6089T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6089 | chr4 | 127838963 | ||||||
| chr4:127839517 | G | A | 1 | a0001c0001t0016 | 3 | HG01433.hp2 HG02273.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6643G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6643 | chr4 | 127839517 | ||||||
| chr4:127839594 | G | A | 1 | a0001c0001t0053 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6720G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6720 | chr4 | 127839594 | ||||||
| chr4:127839718 | G | A | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6844G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 6844 | chr4 | 127839718 | ||||||
| chr4:127840332 | A | T | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(4): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*7458A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 7458 | chr4 | 127840332 | ||||||
| chr4:127840678 | T | G | 1 | a0002c0002t0038 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7804T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 19/19 | 7804 | chr4 | 127840678 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127782795 | C | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
68 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.107+138C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127782795 | |||||||
| chr4:127782882 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.107+225T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127782882 | |||||||
| chr4:127782915 | A | G | 3 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0014g0226 |
3 | NA18747.hp1 NA18947.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.107+258A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127782915 | |||||||
| chr4:127783181 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
113 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.107+538delT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 127783181 | ||||||
| chr4:127783370 | G | C | 49 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0002c0002t0001g0002 others(46): Show |
70 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.107+713G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783370 | |||||||
| chr4:127783456 | T | C | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107+799T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783456 | |||||||
| chr4:127783504 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.107+847C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783504 | |||||||
| chr4:127783648 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107+991C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783648 | |||||||
| chr4:127783727 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.107+1070A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783727 | |||||||
| chr4:127783963 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.107+1306C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127783963 | |||||||
| chr4:127784050 | C | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.107+1393C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784050 | |||||||
| chr4:127784071 | G | A | 1 | a0001c0001t0016g0055 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.107+1414G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784071 | |||||||
| chr4:127784210 | C | T | 1 | a0001c0001t0054g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.107+1553C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784210 | |||||||
| chr4:127784346 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.107+1689G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784346 | |||||||
| chr4:127784543 | C | T | 3 | a0001c0001t0013g0187 a0001c0001t0013g0188 a0001c0001t0013g0189 |
3 | HG01168.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.107+1886C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784543 | |||||||
| chr4:127784692 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+2035C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784692 | |||||||
| chr4:127784696 | C | T | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.107+2039C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784696 | |||||||
| chr4:127784873 | T | C | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107+2216T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127784873 | |||||||
| chr4:127785181 | A | G | 54 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(51): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+2524A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785181 | |||||||
| chr4:127785225 | G | A | 17 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(14): Show |
20 | HG00621.hp1 HG02080.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.107+2568G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785225 | |||||||
| chr4:127785240 | C | T | 10 | a0001c0003t0001g0019 a0001c0003t0001g0045 a0001c0003t0001g0046 others(7): Show |
14 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+2583C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785240 | |||||||
| chr4:127785563 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0054g0190 |
2 | HG01168.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.107+2906G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785563 | |||||||
| chr4:127785581 | G | C | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+2924G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785581 | |||||||
| chr4:127785626 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.107+2969G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785626 | |||||||
| chr4:127785850 | A | C | 1 | a0001c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+3193A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785850 | |||||||
| chr4:127785950 | A | T | 1 | a0001c0001t0024g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.107+3293A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127785950 | |||||||
| chr4:127786088 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.107+3431G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786088 | |||||||
| chr4:127786176 | CT | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
240 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.107+3527delT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 127786176 | ||||||
| chr4:127786187 | G | A | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.107+3530G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786187 | |||||||
| chr4:127786301 | T | G | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+3644T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786301 | |||||||
| chr4:127786316 | A | G | 1 | a0002c0002t0003g0017 | 3 | NA18949.hp2 NA19062.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.107+3659A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786316 | |||||||
| chr4:127786357 | G | A | 3 | a0001c0001t0013g0187 a0001c0001t0013g0188 a0001c0001t0013g0189 |
3 | HG01168.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.107+3700G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786357 | |||||||
| chr4:127786678 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.107+4021G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786678 | |||||||
| chr4:127786846 | A | G | 1 | a0001c0001t0012g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.107+4189A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127786846 | |||||||
| chr4:127787054 | T | G | 70 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(67): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.107+4397T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787054 | |||||||
| chr4:127787197 | A | G | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+4540A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787197 | |||||||
| chr4:127787432 | G | C | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+4775G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787432 | |||||||
| chr4:127787542 | A | G | 1 | a0001c0003t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107+4885A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787542 | |||||||
| chr4:127787622 | T | C | 13 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.107+4965T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787622 | |||||||
| chr4:127787733 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0027g0039 |
2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.107+5076C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787733 | |||||||
| chr4:127787783 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.107+5126C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787783 | |||||||
| chr4:127787870 | G | A | 3 | a0001c0001t0017g0039 a0001c0001t0017g0154 a0001c0001t0027g0039 |
3 | HG01496.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.107+5213G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127787870 | |||||||
| chr4:127788024 | C | T | 1 | a0001c0001t0054g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.107+5367C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788024 | |||||||
| chr4:127788171 | A | G | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107+5514A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788171 | |||||||
| chr4:127788298 | A | G | 3 | a0002c0002t0001g0036 a0002c0002t0001g0136 a0002c0002t0001g0137 |
4 | NA18950.hp2 NA18973.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+5641A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788298 | |||||||
| chr4:127788344 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+5687A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788344 | |||||||
| chr4:127788388 | A | C | 1 | a0001c0003t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108-5689A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788388 | |||||||
| chr4:127788498 | A | T | 1 | a0001c0001t0002g0052 | 2 | HG02523.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.108-5579A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788498 | |||||||
| chr4:127788763 | C | T | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-5314C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788763 | |||||||
| chr4:127788920 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108-5157A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127788920 | |||||||
| chr4:127789048 | G | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.108-5029G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789048 | |||||||
| chr4:127789050 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
240 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.108-5027A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789050 | |||||||
| chr4:127789096 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.108-4981C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789096 | |||||||
| chr4:127789418 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0023 others(17): Show |
27 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.108-4659G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789418 | |||||||
| chr4:127789490 | C | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.108-4587C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789490 | |||||||
| chr4:127789573 | G | T | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4504G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789573 | |||||||
| chr4:127789627 | G | A | 1 | a0001c0001t0053g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108-4450G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127789627 | |||||||
| chr4:127789647 | C | CA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
135 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.108-4419dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 127789647 | ||||||
| chr4:127790158 | A | G | 1 | a0002c0002t0001g0134 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.108-3919A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790158 | |||||||
| chr4:127790272 | T | G | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-3805T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790272 | |||||||
| chr4:127790357 | C | T | 1 | a0001c0001t0053g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108-3720C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790357 | |||||||
| chr4:127790796 | C | T | 1 | a0001c0001t0002g0051 | 2 | NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.108-3281C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790796 | |||||||
| chr4:127790859 | T | C | 1 | a0001c0001t0002g0047 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.108-3218T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790859 | |||||||
| chr4:127790883 | G | C | 1 | a0001c0001t0012g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.108-3194G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127790883 | |||||||
| chr4:127791069 | C | G | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-3008C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791069 | |||||||
| chr4:127791109 | A | G | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-2968A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791109 | |||||||
| chr4:127791157 | TTAATA | T | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-2917_108-2913d others(7): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 127791157 | ||||||
| chr4:127791327 | A | C | 1 | a0001c0001t0055g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.108-2750A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791327 | |||||||
| chr4:127791341 | C | G | 1 | a0001c0005t0007g0184 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-2736C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791341 | |||||||
| chr4:127791409 | C | T | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-2668C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791409 | |||||||
| chr4:127791412 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.108-2665A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791412 | |||||||
| chr4:127791908 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
8 | HG02015.hp1 HG02155.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2169A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127791908 | |||||||
| chr4:127792120 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.108-1957A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127792120 | |||||||
| chr4:127792728 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA19055.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.108-1349A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127792728 | |||||||
| chr4:127792860 | T | C | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-1217T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127792860 | |||||||
| chr4:127792878 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-1199G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127792878 | |||||||
| chr4:127793322 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.108-755T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793322 | |||||||
| chr4:127793358 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
240 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.108-719C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793358 | |||||||
| chr4:127793721 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.108-356G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793721 | |||||||
| chr4:127793781 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.108-296C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793781 | |||||||
| chr4:127793853 | T | C | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.108-224T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793853 | |||||||
| chr4:127793924 | T | G | 1 | a0002c0002t0023g0112 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108-153T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127793924 | |||||||
| chr4:127794004 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.108-73A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 1/18 | chr4 | 127794004 | |||||||
| chr4:127794152 | A | C | 1 | a0001c0001t0002g0223 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.165+18A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127794152 | |||||||
| chr4:127794385 | A | C | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.165+251A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127794385 | |||||||
| chr4:127794454 | A | C | 10 | a0001c0003t0001g0019 a0001c0003t0001g0045 a0001c0003t0001g0046 others(7): Show |
14 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+320A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127794454 | |||||||
| chr4:127794762 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.165+628A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127794762 | |||||||
| chr4:127794928 | G | A | 2 | a0002c0002t0001g0167 a0002c0002t0001g0168 |
2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.165+794G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127794928 | |||||||
| chr4:127795124 | A | G | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-644A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127795124 | |||||||
| chr4:127795130 | A | T | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-638A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127795130 | |||||||
| chr4:127795409 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.166-359G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127795409 | |||||||
| chr4:127795493 | C | T | 1 | a0001c0001t0013g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.166-275C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127795493 | |||||||
| chr4:127795592 | A | G | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.166-176A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 2/18 | chr4 | 127795592 | |||||||
| chr4:127796041 | G | A | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.306+133G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127796041 | |||||||
| chr4:127796482 | A | G | 1 | a0001c0001t0053g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+574A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127796482 | |||||||
| chr4:127797045 | G | T | 1 | a0001c0001t0002g0047 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.306+1137G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797045 | |||||||
| chr4:127797134 | CAG | C | 3 | a0001c0001t0017g0039 a0001c0001t0017g0154 a0001c0001t0027g0039 |
3 | HG01496.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.306+1227_306+1228d others(4): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797134 | |||||||
| chr4:127797324 | A | C | 1 | a0001c0001t0002g0022 | 3 | NA18943.hp2 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.307-1263A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797324 | |||||||
| chr4:127797358 | T | C | 1 | a0002c0002t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.307-1229T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797358 | |||||||
| chr4:127797378 | A | G | 1 | a0002c0002t0001g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-1209A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797378 | |||||||
| chr4:127797602 | A | AT | 98 | a0001c0001t0001g0099 a0001c0001t0001g0135 a0001c0001t0001g0138 others(95): Show |
133 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.307-968dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 127797602 | ||||||
| chr4:127797602 | A | T | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-985A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797602 | |||||||
| chr4:127797625 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.307-962G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797625 | |||||||
| chr4:127797752 | C | A | 3 | a0001c0001t0013g0187 a0001c0001t0013g0188 a0001c0001t0013g0189 |
3 | HG01168.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.307-835C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797752 | |||||||
| chr4:127797871 | G | A | 1 | a0001c0001t0012g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.307-716G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797871 | |||||||
| chr4:127797884 | A | G | 69 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(66): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.307-703A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797884 | |||||||
| chr4:127797921 | A | G | 69 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(66): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.307-666A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797921 | |||||||
| chr4:127797940 | T | C | 6 | a0001c0001t0001g0025 a0003c0004t0001g0024 a0003c0004t0001g0025 others(3): Show |
6 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-647T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797940 | |||||||
| chr4:127797984 | C | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.307-603C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127797984 | |||||||
| chr4:127798014 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.307-573A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127798014 | |||||||
| chr4:127798159 | T | G | 1 | a0002c0002t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.307-428T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127798159 | |||||||
| chr4:127798214 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0040g0097 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.307-373C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127798214 | |||||||
| chr4:127798360 | A | G | 1 | a0001c0003t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.307-227A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 3/18 | chr4 | 127798360 | |||||||
| chr4:127798858 | T | G | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+149T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127798858 | |||||||
| chr4:127798908 | C | T | 5 | a0001c0001t0015g0041 a0001c0001t0015g0161 a0001c0001t0042g0162 others(2): Show |
6 | HG01109.hp2 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+199C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127798908 | |||||||
| chr4:127799429 | C | T | 2 | a0001c0005t0007g0182 a0001c0005t0007g0183 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.429+720C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127799429 | |||||||
| chr4:127799465 | C | G | 1 | a0001c0001t0017g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.429+756C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127799465 | |||||||
| chr4:127799587 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.429+878T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127799587 | |||||||
| chr4:127799606 | A | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
128 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.429+897A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127799606 | |||||||
| chr4:127799738 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0043g0031 |
2 | HG02004.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.429+1029G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127799738 | |||||||
| chr4:127800145 | G | C | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.430-993G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800145 | |||||||
| chr4:127800166 | G | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0174 |
3 | HG02109.hp2 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.430-972G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800166 | |||||||
| chr4:127800173 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.430-965A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800173 | |||||||
| chr4:127800188 | C | G | 1 | a0001c0001t0029g0096 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.430-950C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800188 | |||||||
| chr4:127800288 | G | A | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.430-850G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800288 | |||||||
| chr4:127800399 | T | A | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-739T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800399 | |||||||
| chr4:127800410 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.430-728G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800410 | |||||||
| chr4:127800744 | C | T | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-394C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800744 | |||||||
| chr4:127800941 | A | G | 1 | a0001c0003t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.430-197A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127800941 | |||||||
| chr4:127801021 | T | C | 47 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.430-117T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127801021 | |||||||
| chr4:127801110 | A | G | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.430-28A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 4/18 | chr4 | 127801110 | |||||||
| chr4:127801458 | C | CGT | 6 | a0001c0001t0002g0219 a0001c0001t0005g0140 a0001c0001t0005g0141 others(3): Show |
6 | HG02074.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+264_529+265dup others(2): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | C | CGTGTGT | 6 | a0001c0001t0005g0037 a0001c0001t0005g0142 a0001c0001t0005g0143 others(3): Show |
6 | HG02257.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+260_529+265dup others(6): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0005g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.529+256_529+265dup others(10): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGT | C | 77 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(74): Show |
114 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.529+264_529+265del others(2): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGT | C | 16 | a0001c0001t0002g0196 a0001c0001t0002g0198 a0001c0001t0002g0220 others(13): Show |
24 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.529+262_529+265del others(4): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGTGT | C | 18 | a0001c0001t0002g0048 a0001c0001t0002g0195 a0001c0001t0012g0151 others(15): Show |
23 | HG01109.hp2 HG01168.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.529+260_529+265del others(6): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGTGTG others(1): Show |
C | 17 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0186 others(14): Show |
18 | HG00741.hp2 HG01175.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+258_529+265del others(8): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGTGTG others(3): Show |
C | 7 | a0001c0001t0001g0098 a0001c0001t0052g0185 a0001c0003t0001g0165 others(4): Show |
8 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+256_529+265del others(10): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGTGTG others(5): Show |
C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(5): Show |
8 | HG02886.hp1 HG03195.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+254_529+265del others(12): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801458 | CGTGTGTG others(7): Show |
C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.529+252_529+265del others(14): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 127801458 | ||||||
| chr4:127801499 | G | A | 47 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0010 others(44): Show |
68 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.529+262G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | chr4 | 127801499 | |||||||
| chr4:127801525 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.530-260G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 5/18 | chr4 | 127801525 | |||||||
| chr4:127802303 | T | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(6): Show |
10 | HG01109.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.663+385T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127802303 | |||||||
| chr4:127802789 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.664-840G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127802789 | |||||||
| chr4:127802819 | T | C | 1 | a0002c0002t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.664-810T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127802819 | |||||||
| chr4:127802864 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0015g0041 a0001c0003t0001g0175 |
4 | HG01109.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-765T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127802864 | |||||||
| chr4:127802983 | G | T | 1 | a0002c0002t0032g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.664-646G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127802983 | |||||||
| chr4:127803112 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
127 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.664-517G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127803112 | |||||||
| chr4:127803217 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.664-412A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127803217 | |||||||
| chr4:127803314 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.664-315T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127803314 | |||||||
| chr4:127803324 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.664-305T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127803324 | |||||||
| chr4:127803360 | A | AGTT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
245 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.664-266_664-264dup others(3): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 127803360 | ||||||
| chr4:127803520 | T | C | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.664-109T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 6/18 | chr4 | 127803520 | |||||||
| chr4:127803906 | T | G | 2 | a0001c0003t0001g0019 a0001c0003t0001g0180 |
4 | HG00735.hp2 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+33T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 7/18 | chr4 | 127803906 | |||||||
| chr4:127804146 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985+59G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804146 | |||||||
| chr4:127804259 | C | G | 1 | a0002c0002t0038g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.985+172C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804259 | |||||||
| chr4:127804364 | G | A | 9 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(6): Show |
10 | HG01109.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.985+277G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804364 | |||||||
| chr4:127804476 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.985+389C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804476 | |||||||
| chr4:127804527 | A | G | 1 | a0001c0003t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.985+440A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804527 | |||||||
| chr4:127804608 | A | AAC | 9 | a0001c0001t0001g0159 a0001c0001t0015g0161 a0001c0001t0055g0164 others(6): Show |
15 | HG01256.hp1 HG01258.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.986-426_986-425dup others(2): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | A | AACAC | 7 | a0001c0001t0001g0186 a0001c0001t0017g0039 a0001c0001t0017g0154 others(4): Show |
7 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-428_986-425dup others(4): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AAC | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0081 others(14): Show |
17 | HG01168.hp1 HG01192.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.986-426_986-425del others(2): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AACAC | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.986-428_986-425del others(4): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AACACAC | A | 48 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0068 others(45): Show |
68 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.986-430_986-425del others(6): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AACACACA others(1): Show |
A | 6 | a0001c0001t0002g0050 a0001c0001t0002g0198 a0001c0001t0002g0211 others(3): Show |
7 | HG01081.hp1 HG01978.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-432_986-425del others(8): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AACACACA others(3): Show |
A | 8 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0141 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-434_986-425del others(10): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804608 | AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0158 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.986-440_986-425del others(16): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804608 | ||||||
| chr4:127804630 | C | CACACACA others(1): Show |
2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.986-436_986-435ins others(8): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804630 | ||||||
| chr4:127804630 | C | CACACAG | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-438_986-437ins others(6): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 127804630 | ||||||
| chr4:127804630 | C | T | 1 | a0001c0001t0008g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.986-443C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804630 | |||||||
| chr4:127804672 | G | T | 1 | a0001c0001t0002g0047 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.986-401G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 8/18 | chr4 | 127804672 | |||||||
| chr4:127805431 | A | G | 1 | a0001c0005t0007g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1137+207A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 9/18 | chr4 | 127805431 | |||||||
| chr4:127806405 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1244+612G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806405 | |||||||
| chr4:127806408 | A | G | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+615A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806408 | |||||||
| chr4:127806565 | A | T | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+772A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806565 | |||||||
| chr4:127806600 | T | A | 1 | a0001c0003t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244+807T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806600 | |||||||
| chr4:127806663 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1244+870A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806663 | |||||||
| chr4:127806847 | C | T | 1 | a0001c0005t0007g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1244+1054C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127806847 | |||||||
| chr4:127807293 | T | C | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1245-703T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807293 | |||||||
| chr4:127807313 | TA | T | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1245-682delA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807313 | |||||||
| chr4:127807411 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1245-585A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807411 | |||||||
| chr4:127807463 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1245-533G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807463 | |||||||
| chr4:127807708 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1245-288G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807708 | |||||||
| chr4:127807912 | A | G | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1245-84A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 10/18 | chr4 | 127807912 | |||||||
| chr4:127808186 | T | A | 2 | a0002c0002t0001g0120 a0002c0002t0001g0121 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1378+57T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127808186 | |||||||
| chr4:127808658 | G | A | 1 | a0001c0001t0012g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1378+529G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127808658 | |||||||
| chr4:127808723 | G | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0022 |
7 | NA18942.hp2 NA18943.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+594G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127808723 | |||||||
| chr4:127808841 | C | G | 1 | a0001c0001t0001g0016 | 3 | HG00609.hp2 HG02056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1378+712C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127808841 | |||||||
| chr4:127808984 | A | AAACTT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
221 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.1378+856_1378+860d others(7): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr4 | 127808984 | ||||||
| chr4:127808997 | T | C | 1 | a0002c0002t0050g0107 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1378+868T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127808997 | |||||||
| chr4:127809000 | A | G | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1378+871A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127809000 | |||||||
| chr4:127809295 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1378+1166G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127809295 | |||||||
| chr4:127809345 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1378+1216G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127809345 | |||||||
| chr4:127810243 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1379-1194A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810243 | |||||||
| chr4:127810325 | T | C | 3 | a0001c0001t0015g0041 a0001c0001t0015g0161 a0001c0001t0042g0162 |
4 | HG01109.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-1112T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810325 | |||||||
| chr4:127810348 | C | T | 1 | a0002c0002t0001g0035 | 2 | NA18947.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1379-1089C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810348 | |||||||
| chr4:127810372 | C | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1379-1065C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810372 | |||||||
| chr4:127810390 | A | G | 13 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1379-1047A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810390 | |||||||
| chr4:127810559 | A | T | 1 | a0001c0001t0002g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1379-878A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127810559 | |||||||
| chr4:127811044 | A | C | 1 | a0001c0001t0002g0223 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1379-393A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127811044 | |||||||
| chr4:127811168 | A | C | 1 | a0002c0002t0009g0033 | 2 | NA19009.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1379-269A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127811168 | |||||||
| chr4:127811179 | C | CT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1379-244dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr4 | 127811179 | ||||||
| chr4:127811242 | A | G | 1 | a0001c0001t0005g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1379-195A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127811242 | |||||||
| chr4:127811341 | T | G | 1 | a0001c0001t0012g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1379-96T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 11/18 | chr4 | 127811341 | |||||||
| chr4:127811771 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
227 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.1578+135A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127811771 | |||||||
| chr4:127811920 | C | T | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1578+284C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127811920 | |||||||
| chr4:127812176 | G | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0022 others(3): Show |
13 | NA18942.hp2 NA18943.hp2 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.1578+540G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812176 | |||||||
| chr4:127812233 | C | T | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1578+597C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812233 | |||||||
| chr4:127812408 | C | CA | 52 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0002g0007 others(49): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1578+784dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127812408 | ||||||
| chr4:127812418 | A | AC | 5 | a0001c0001t0002g0212 a0001c0001t0002g0217 a0001c0001t0022g0207 others(2): Show |
5 | HG00558.hp1 HG00738.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+782_1578+783i others(3): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812418 | |||||||
| chr4:127812421 | C | A | 2 | a0001c0001t0002g0201 a0002c0002t0001g0137 |
2 | NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1578+785C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812421 | |||||||
| chr4:127812422 | A | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(4): Show |
8 | HG01109.hp2 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+786A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812422 | |||||||
| chr4:127812479 | T | C | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+843T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812479 | |||||||
| chr4:127812520 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1578+884G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812520 | |||||||
| chr4:127812697 | A | AT | 6 | a0001c0001t0015g0041 a0001c0001t0015g0161 a0001c0001t0042g0162 others(3): Show |
7 | HG01109.hp2 HG01358.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+1076dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127812697 | ||||||
| chr4:127812697 | AT | A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0103 a0001c0001t0002g0203 others(3): Show |
6 | HG02273.hp1 NA18948.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578+1076delT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127812697 | ||||||
| chr4:127812700 | T | A | 11 | a0001c0001t0002g0213 a0001c0001t0005g0037 a0001c0001t0005g0139 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578+1064T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127812700 | |||||||
| chr4:127812718 | C | CTAT | 70 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(67): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1578+1083_1578+108 others(7): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127812718 | ||||||
| chr4:127813004 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1578+1368T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813004 | |||||||
| chr4:127813100 | T | C | 7 | a0001c0001t0001g0135 a0002c0002t0001g0010 a0002c0002t0001g0122 others(4): Show |
9 | NA18954.hp1 NA18955.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.1578+1464T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813100 | |||||||
| chr4:127813114 | C | T | 70 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(67): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1578+1478C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813114 | |||||||
| chr4:127813145 | A | T | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1578+1509A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813145 | |||||||
| chr4:127813169 | G | T | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1578+1533G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813169 | |||||||
| chr4:127813288 | G | A | 1 | a0001c0001t0017g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1578+1652G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813288 | |||||||
| chr4:127813353 | C | G | 4 | a0003c0004t0001g0024 a0003c0004t0020g0075 a0003c0004t0020g0076 others(1): Show |
4 | HG00099.hp2 HG01192.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+1717C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813353 | |||||||
| chr4:127813430 | C | G | 1 | a0001c0001t0008g0083 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1578+1794C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813430 | |||||||
| chr4:127813501 | ATAAT | A | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+1867_1578+187 others(8): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127813501 | ||||||
| chr4:127813533 | A | G | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+1897A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813533 | |||||||
| chr4:127813674 | G | T | 1 | a0001c0003t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1578+2038G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813674 | |||||||
| chr4:127813809 | A | T | 1 | a0001c0003t0001g0046 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1578+2173A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127813809 | |||||||
| chr4:127814088 | TTGTC | T | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+2456_1578+245 others(8): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127814088 | ||||||
| chr4:127814122 | TTAAAGG | T | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1578+2487_1578+249 others(10): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814122 | |||||||
| chr4:127814155 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0035g0023 a0001c0008t0044g0062 |
3 | HG02155.hp1 NA18747.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1578+2519G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814155 | |||||||
| chr4:127814235 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1578+2599G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814235 | |||||||
| chr4:127814320 | A | G | 47 | a0001c0001t0001g0135 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
68 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1578+2684A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814320 | |||||||
| chr4:127814606 | C | T | 1 | a0001c0003t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1578+2970C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814606 | |||||||
| chr4:127814613 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1578+2977G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814613 | |||||||
| chr4:127814642 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1578+3006G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814642 | |||||||
| chr4:127814818 | A | G | 1 | a0001c0001t0013g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1578+3182A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814818 | |||||||
| chr4:127814981 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0030 |
6 | HG02074.hp2 HG02083.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-3344A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127814981 | |||||||
| chr4:127815125 | A | C | 1 | a0001c0001t0002g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1579-3200A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127815125 | |||||||
| chr4:127815252 | A | G | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1579-3073A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127815252 | |||||||
| chr4:127815449 | G | A | 7 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(4): Show |
8 | HG01109.hp2 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-2876G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127815449 | |||||||
| chr4:127815491 | C | CA | 9 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0102 others(6): Show |
9 | HG00544.hp1 HG01175.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-2819dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127815491 | ||||||
| chr4:127815701 | A | G | 1 | a0001c0005t0007g0183 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1579-2624A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127815701 | |||||||
| chr4:127815934 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1579-2391G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127815934 | |||||||
| chr4:127816093 | C | T | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1579-2232C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127816093 | |||||||
| chr4:127816246 | C | G | 1 | a0001c0001t0008g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1579-2079C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127816246 | |||||||
| chr4:127816344 | T | C | 57 | a0001c0001t0001g0135 a0002c0002t0001g0002 a0002c0002t0001g0003 others(54): Show |
81 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1579-1981T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127816344 | |||||||
| chr4:127817129 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0077 others(6): Show |
11 | HG00642.hp2 HG01070.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579-1196G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817129 | |||||||
| chr4:127817177 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1579-1148G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817177 | |||||||
| chr4:127817211 | G | A | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1579-1114G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817211 | |||||||
| chr4:127817265 | C | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1579-1060C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817265 | |||||||
| chr4:127817333 | T | C | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1579-992T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817333 | |||||||
| chr4:127817348 | C | CA | 8 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(5): Show |
9 | HG01109.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579-965dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127817348 | ||||||
| chr4:127817348 | CA | C | 54 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(51): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1579-965delA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 127817348 | ||||||
| chr4:127817408 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1579-917G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817408 | |||||||
| chr4:127817629 | T | A | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1579-696T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817629 | |||||||
| chr4:127817864 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1579-461A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817864 | |||||||
| chr4:127817883 | A | G | 1 | a0002c0002t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1579-442A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817883 | |||||||
| chr4:127817954 | C | A | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1579-371C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127817954 | |||||||
| chr4:127818188 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0030 others(8): Show |
18 | HG01433.hp2 HG02074.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579-137T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127818188 | |||||||
| chr4:127818278 | A | G | 54 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(51): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1579-47A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127818278 | |||||||
| chr4:127818293 | C | A | 1 | a0001c0006t0011g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1579-32C>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 12/18 | chr4 | 127818293 | |||||||
| chr4:127818772 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1674+352C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127818772 | |||||||
| chr4:127818948 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1674+528A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127818948 | |||||||
| chr4:127819014 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1674+594A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127819014 | |||||||
| chr4:127819094 | G | A | 70 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(67): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1674+674G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127819094 | |||||||
| chr4:127819219 | G | A | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1674+799G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127819219 | |||||||
| chr4:127819560 | T | G | 2 | a0001c0001t0017g0039 a0001c0001t0027g0039 |
2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1675-868T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127819560 | |||||||
| chr4:127819737 | AT | A | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675-688delT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 127819737 | ||||||
| chr4:127819790 | A | G | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-638A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127819790 | |||||||
| chr4:127820198 | G | A | 1 | a0002c0002t0004g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1675-230G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127820198 | |||||||
| chr4:127820338 | A | G | 50 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(47): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1675-90A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 13/18 | chr4 | 127820338 | |||||||
| chr4:127820899 | T | C | 1 | a0001c0001t0014g0224 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1812+334T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127820899 | |||||||
| chr4:127820993 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1812+428T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127820993 | |||||||
| chr4:127821135 | G | C | 2 | a0001c0001t0022g0207 a0001c0001t0048g0208 |
2 | HG00558.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1812+570G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821135 | |||||||
| chr4:127821243 | A | T | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1812+678A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821243 | |||||||
| chr4:127821409 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1812+844T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821409 | |||||||
| chr4:127821468 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1812+903C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821468 | |||||||
| chr4:127821615 | T | G | 4 | a0001c0001t0002g0020 a0001c0001t0002g0051 a0001c0001t0002g0200 others(1): Show |
6 | NA18960.hp1 NA18974.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1812+1050T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821615 | |||||||
| chr4:127821991 | T | C | 3 | a0001c0001t0017g0039 a0001c0001t0017g0154 a0001c0001t0027g0039 |
3 | HG01496.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1813-778T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127821991 | |||||||
| chr4:127822083 | T | C | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1813-686T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822083 | |||||||
| chr4:127822332 | G | A | 1 | a0002c0002t0009g0123 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1813-437G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822332 | |||||||
| chr4:127822332 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1813-437G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822332 | |||||||
| chr4:127822463 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(1): Show |
4 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-306G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822463 | |||||||
| chr4:127822484 | T | A | 1 | a0001c0001t0002g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1813-285T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822484 | |||||||
| chr4:127822507 | T | C | 1 | a0001c0003t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1813-262T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822507 | |||||||
| chr4:127822718 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1813-51A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822718 | |||||||
| chr4:127822718 | A | G | 1 | a0002c0002t0004g0150 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1813-51A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 14/18 | chr4 | 127822718 | |||||||
| chr4:127823242 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1939-275G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 15/18 | chr4 | 127823242 | |||||||
| chr4:127823387 | G | A | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-130G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 15/18 | chr4 | 127823387 | |||||||
| chr4:127823463 | CT | C | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939-50delT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 127823463 | ||||||
| chr4:127823473 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1939-44T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 15/18 | chr4 | 127823473 | |||||||
| chr4:127823688 | GAGCAC | G | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2046+67_2046+71del others(5): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 127823688 | ||||||
| chr4:127823721 | TTTAA | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2046+100_2046+103d others(6): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 127823721 | ||||||
| chr4:127823739 | T | G | 1 | a0001c0001t0052g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2046+115T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127823739 | |||||||
| chr4:127824153 | G | A | 1 | a0002c0002t0003g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2046+529G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824153 | |||||||
| chr4:127824202 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
128 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2046+578C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824202 | |||||||
| chr4:127824400 | G | A | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2046+776G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824400 | |||||||
| chr4:127824490 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(1): Show |
4 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+866G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824490 | |||||||
| chr4:127824644 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2046+1020C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824644 | |||||||
| chr4:127824952 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0010g0020 |
3 | NA18960.hp1 NA18983.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2046+1328T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127824952 | |||||||
| chr4:127825151 | A | C | 1 | a0001c0001t0002g0219 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2046+1527A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825151 | |||||||
| chr4:127825189 | C | T | 15 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(12): Show |
16 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2046+1565C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825189 | |||||||
| chr4:127825450 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2046+1826G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825450 | |||||||
| chr4:127825450 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2046+1826G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825450 | |||||||
| chr4:127825682 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2047-1623A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825682 | |||||||
| chr4:127825783 | G | A | 1 | a0002c0002t0001g0137 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2047-1522G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825783 | |||||||
| chr4:127825787 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2047-1518A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825787 | |||||||
| chr4:127825926 | CA | C | 8 | a0001c0001t0001g0094 a0001c0001t0018g0018 a0001c0001t0031g0018 others(5): Show |
9 | HG01070.hp1 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2047-1361delA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 127825926 | ||||||
| chr4:127825938 | A | G | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-1367A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127825938 | |||||||
| chr4:127826013 | A | G | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-1292A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127826013 | |||||||
| chr4:127826083 | C | G | 2 | a0001c0001t0008g0082 a0001c0001t0008g0083 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2047-1222C>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127826083 | |||||||
| chr4:127826117 | A | T | 1 | a0001c0001t0054g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2047-1188A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127826117 | |||||||
| chr4:127826401 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
240 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.2047-904G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127826401 | |||||||
| chr4:127826827 | A | G | 2 | a0001c0001t0018g0018 a0001c0001t0031g0018 |
3 | HG02145.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2047-478A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 16/18 | chr4 | 127826827 | |||||||
| chr4:127827691 | TTGTTTTC others(21): Show |
T | 1 | a0001c0001t0045g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2166+274_2166+301d others(30): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 127827691 | ||||||
| chr4:127827797 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2166+373G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127827797 | |||||||
| chr4:127827944 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2166+520G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127827944 | |||||||
| chr4:127828088 | T | G | 1 | a0001c0001t0012g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2166+664T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828088 | |||||||
| chr4:127828128 | T | C | 2 | a0001c0001t0005g0037 a0001c0001t0025g0037 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2166+704T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828128 | |||||||
| chr4:127828274 | T | C | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2166+850T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828274 | |||||||
| chr4:127828418 | T | G | 1 | a0002c0002t0037g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2166+994T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828418 | |||||||
| chr4:127828580 | T | C | 1 | a0001c0003t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2166+1156T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828580 | |||||||
| chr4:127828856 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2166+1432A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828856 | |||||||
| chr4:127828977 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0027g0039 |
2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2166+1553T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127828977 | |||||||
| chr4:127829029 | G | T | 10 | a0001c0001t0005g0037 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2166+1605G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829029 | |||||||
| chr4:127829129 | A | C | 1 | a0001c0001t0002g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2167-1509A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829129 | |||||||
| chr4:127829519 | C | T | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2167-1119C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829519 | |||||||
| chr4:127829786 | A | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(44): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.2167-852A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829786 | |||||||
| chr4:127829793 | A | G | 54 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(51): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2167-845A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829793 | |||||||
| chr4:127829873 | ATG | A | 3 | a0001c0001t0017g0039 a0001c0001t0017g0154 a0001c0001t0027g0039 |
3 | HG01496.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2167-762_2167-761d others(4): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 127829873 | ||||||
| chr4:127829927 | CAGA | C | 30 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0020 others(27): Show |
45 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.2167-708_2167-706d others(5): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 127829927 | ||||||
| chr4:127829930 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0092 others(2): Show |
6 | HG00639.hp2 HG01346.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2167-708A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829930 | |||||||
| chr4:127829986 | G | GT | 49 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(46): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2167-644dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 127829986 | ||||||
| chr4:127829994 | T | C | 2 | a0001c0006t0011g0040 a0001c0006t0011g0155 |
3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2167-644T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127829994 | |||||||
| chr4:127830175 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2167-463C>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127830175 | |||||||
| chr4:127830178 | T | G | 1 | a0002c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2167-460T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127830178 | |||||||
| chr4:127830218 | CTCT | C | 3 | a0001c0001t0013g0187 a0001c0001t0013g0188 a0001c0001t0013g0189 |
3 | HG01168.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2167-414_2167-412d others(5): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 127830218 | ||||||
| chr4:127830446 | T | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2167-192T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127830446 | |||||||
| chr4:127830631 | T | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0205 |
2 | NA19066.hp2 NA19078.hp2 |
splice_region_variant&intron_variant | LOW | c.2167-7T>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 17/18 | chr4 | 127830631 | |||||||
| chr4:127830918 | T | G | 4 | a0001c0001t0002g0020 a0001c0001t0002g0051 a0001c0001t0002g0200 others(1): Show |
6 | NA18960.hp1 NA18974.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2328+119T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127830918 | |||||||
| chr4:127831049 | T | G | 1 | a0001c0001t0001g0030 | 2 | HG02074.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2328+250T>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831049 | |||||||
| chr4:127831144 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2328+345G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831144 | |||||||
| chr4:127831259 | G | C | 6 | a0001c0001t0012g0151 a0001c0001t0012g0152 a0001c0001t0012g0153 others(3): Show |
6 | HG01168.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2328+460G>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831259 | |||||||
| chr4:127831259 | G | T | 6 | a0001c0001t0018g0018 a0001c0001t0031g0018 a0001c0005t0007g0181 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2328+460G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831259 | |||||||
| chr4:127831373 | T | C | 4 | a0001c0005t0007g0181 a0001c0005t0007g0182 a0001c0005t0007g0183 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2328+574T>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831373 | |||||||
| chr4:127831468 | G | T | 70 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(67): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2328+669G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831468 | |||||||
| chr4:127831479 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0066 |
2 | HG00642.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2328+680G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831479 | |||||||
| chr4:127831499 | A | AT | 41 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(38): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2328+702dupT | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 127831499 | ||||||
| chr4:127831501 | T | TA | 16 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0111 others(13): Show |
20 | HG00099.hp1 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.2328+724dupA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 127831501 | ||||||
| chr4:127831501 | TA | T | 43 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0094 others(40): Show |
50 | HG00621.hp1 HG01070.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.2328+724delA | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 127831501 | ||||||
| chr4:127831502 | A | T | 5 | a0001c0001t0002g0204 a0001c0001t0002g0211 a0001c0001t0002g0223 others(2): Show |
6 | HG01981.hp2 NA18747.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2328+703A>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831502 | |||||||
| chr4:127831518 | AAAAAAGG others(563): Show |
A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0069 others(2): Show |
10 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(7): Show |
intron_variant | MODIFIER | c.2328+723_2329-592d others(2): Show |
HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 127831518 | ||||||
| chr4:127831524 | G | A | 48 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2328+725G>A | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127831524 | |||||||
| chr4:127832552 | G | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0163 others(1): Show |
4 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2329-131G>T | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127832552 | |||||||
| chr4:127832600 | A | C | 1 | a0001c0001t0002g0201 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2329-83A>C | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127832600 | |||||||
| chr4:127832602 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2329-81A>G | HSPA4L | ENSG00000164070.12 | transcript | ENST00000296464.9 | protein_coding | 18/18 | chr4 | 127832602 |