Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124535 |
| ensemblid | ENSG00000176160.11 |
| hgncid | 26862 |
| symbol | HSF5 |
| name | heat shock transcription factor 5 |
| refseq_nuc | NM_001080439.3 |
| refseq_prot | NP_001073908.2 |
| ensembl_nuc | ENST00000323777.8 |
| ensembl_prot | ENSP00000313243.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 58420167 |
| end | 58488408 |
| strand | - |
| ver | v1.2 |
| region | chr17:58420167-58488408 |
| region5000 | chr17:58415167-58493408 |
| regionname0 | HSF5_chr17_58420167_58488408 |
| regionname5000 | HSF5_chr17_58415167_58493408 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 596 | 266 | 77 | 54 | 95 | 9 | 29 | 71 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0002 | 0/0 | 596 | 57 | 0 | 12 | 37 | 3 | 5 | 31 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0003 | 0/0 | 598 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(593): Show |
chr17 | 58415167 | 58493408 |
| a0004 | 0/0 | 596 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0005 | 0/0 | 596 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0006 | 0/0 | 596 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0007 | 0/0 | 596 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0008 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| a0009 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | MEALL others(591): Show |
chr17 | 58415167 | 58493408 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1788 | 262 | 73 | 54 | 95 | 9 | 29 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0001c0004 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0001c0005 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0002c0002 | 0/0 | 1788 | 57 | 0 | 12 | 37 | 3 | 5 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0003c0003 | 0/0 | 1794 | 3 | 1 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1789): Show |
chr17 | 58415167 | 58493408 | ||
| a0004c0007 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0005c0009 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0006c0011 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0007c0006 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0008c0010 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 | ||
| a0009c0008 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | ATGGA others(1783): Show |
chr17 | 58415167 | 58493408 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4118 | 248 | 69 | 53 | 90 | 8 | 26 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0002 | 0/0 | 4118 | 4 | 0 | 0 | 4 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0003 | 0/0 | 4118 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0004 | 0/0 | 4118 | 2 | 0 | 0 | 0 | 0 | 2 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0005 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0006 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0007 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0009 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0001t0010 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0004t0001 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0001c0005t0001 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0002c0002t0001 | 0/0 | 4118 | 57 | 0 | 12 | 37 | 3 | 5 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0003c0003t0001 | 0/0 | 4124 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4119): Show |
chr17 | 58415167 | 58493408 |
| a0003c0003t0008 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4119): Show |
chr17 | 58415167 | 58493408 |
| a0004c0007t0001 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0005c0009t0001 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0006c0011t0001 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0007c0006t0001 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0008c0010t0001 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| a0009c0008t0001 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | GTGCG others(4113): Show |
chr17 | 58415167 | 58493408 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0003c0003t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0003c0003t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0004c0007t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0005c0009t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0006c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0007c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0008c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| a0009c0008t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0251 | EUR | GBR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0301 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0242 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0015 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0015 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01261 | hp2 | a0004 | c0007 | t0001 | g0195 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01358 | hp1 | a0005 | c0009 | t0001 | g0130 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0233 | EUR | IBS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0069 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03017 | hp1 | a0006 | c0011 | t0001 | g0226 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03654 | hp1 | a0007 | c0006 | t0001 | g0220 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0234 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0182 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0315 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0194 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0265 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0167 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19007 | hp1 | a0008 | c0010 | t0001 | g0047 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19083 | hp1 | a0009 | c0008 | t0001 | g0067 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0313 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20129 | hp2 | a0003 | c0003 | t0008 | g0316 | AFR | ASW | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0240 | SAS | GIH | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0210 | SAS | GIH | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0151 | REF | REF | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58458785 | T | G | 1 | a0009 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1703A>C | p.Gln568Pro | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1837/4118 | 1703/1791 | 568/596 | chr17 | 58458785 | |||
| chr17:58458896 | G | A | 1 | a0005 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1592C>T | p.Pro531Leu | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1726/4118 | 1592/1791 | 531/596 | chr17 | 58458896 | |||
| chr17:58458933 | T | C | 1 | a0008 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.1555A>G | p.Ile519Val | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1689/4118 | 1555/1791 | 519/596 | chr17 | 58458933 | |||
| chr17:58462785 | G | T | 1 | a0004 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1539C>A | p.His513Gln | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/6 | 1673/4118 | 1539/1791 | 513/596 | chr17 | 58462785 | |||
| chr17:58462906 | C | T | 3 | a0002 a0006 a0007 |
59 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(56): Show |
missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/6 | 1552/4118 | 1418/1791 | 473/596 | chr17 | 58462906 | |||
| chr17:58480000 | G | A | 1 | a0006 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.818C>T | p.Thr273Ile | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 952/4118 | 818/1791 | 273/596 | chr17 | 58480000 | |||
| chr17:58480184 | C | T | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.634G>A | p.Asp212Asn | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 768/4118 | 634/1791 | 212/596 | chr17 | 58480184 | |||
| chr17:58488072 | T | TCGGCCC | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
conservative_inframe_insertion | MODERATE | c.197_202dupGGGCCG | p.Gly66_Ala67dup | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/6 | 336/4118 | 202/1791 | 68/596 | chr17 | 58488072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58466906 | A | G | 1 | a0001c0004 | 2 | NA18906.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.999T>C | p.Tyr333Tyr | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/6 | 1133/4118 | 999/1791 | 333/596 | chr17 | 58466906 | |||
| chr17:58480020 | G | A | 1 | a0001c0005 | 2 | HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.798C>T | p.Thr266Thr | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 932/4118 | 798/1791 | 266/596 | chr17 | 58480020 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58420358 | T | C | 1 | a0003c0003t0008 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 2002 | chr17 | 58420358 | ||||||
| chr17:58420528 | T | C | 1 | a0001c0001t0004 | 2 | HG04184.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1832 | chr17 | 58420528 | ||||||
| chr17:58420559 | T | C | 1 | a0001c0001t0009 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1801 | chr17 | 58420559 | ||||||
| chr17:58420600 | T | A | 1 | a0001c0001t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1760 | chr17 | 58420600 | ||||||
| chr17:58421027 | G | A | 1 | a0001c0001t0002 | 4 | NA18939.hp2 NA18954.hp1 NA19000.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1333C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1333 | chr17 | 58421027 | ||||||
| chr17:58421669 | C | T | 1 | a0001c0001t0003 | 2 | HG00323.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*691G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 691 | chr17 | 58421669 | ||||||
| chr17:58422160 | G | C | 1 | a0001c0001t0005 | 2 | HG02451.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 200 | chr17 | 58422160 | ||||||
| chr17:58422311 | C | T | 1 | a0001c0001t0007 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 49 | chr17 | 58422311 | ||||||
| chr17:58488277 | C | T | 1 | a0001c0001t0006 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/6 | 3 | chr17 | 58488277 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58422471 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0104 a0001c0001t0001g0107 others(3): Show |
7 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-41A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422471 | |||||||
| chr17:58422481 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1721-51A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422481 | |||||||
| chr17:58422688 | A | C | 3 | a0002c0002t0001g0224 a0002c0002t0001g0257 a0002c0002t0001g0259 |
3 | NA18612.hp2 NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1721-258T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422688 | |||||||
| chr17:58422694 | CT | C | 145 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0040 others(142): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1721-265delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422694 | |||||||
| chr17:58422694 | CTT | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0048 others(7): Show |
10 | HG00558.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721-266_1721-265d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422694 | |||||||
| chr17:58422718 | G | A | 1 | a0001c0001t0010g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1721-288C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422718 | |||||||
| chr17:58422735 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1721-305C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422735 | |||||||
| chr17:58422798 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-368A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422798 | |||||||
| chr17:58422856 | C | T | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-426G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422856 | |||||||
| chr17:58423101 | T | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 |
3 | HG00642.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1721-671A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423101 | |||||||
| chr17:58423275 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0292 a0001c0001t0010g0017 |
3 | HG02257.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1721-845T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423275 | |||||||
| chr17:58423290 | G | A | 2 | a0001c0001t0004g0194 a0001c0001t0004g0210 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1721-860C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423290 | |||||||
| chr17:58423291 | GTTCA | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
7 | HG02055.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1721-865_1721-862d others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423291 | |||||||
| chr17:58423483 | C | CT | 72 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0024 others(69): Show |
75 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1721-1054dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423483 | |||||||
| chr17:58423483 | CT | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0115 others(6): Show |
12 | HG01070.hp1 HG01081.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1721-1054delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423483 | |||||||
| chr17:58423537 | G | A | 67 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0225 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1721-1107C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423537 | |||||||
| chr17:58423570 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-1140G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423570 | |||||||
| chr17:58423608 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-1178A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423608 | |||||||
| chr17:58423653 | A | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(2): Show |
5 | HG00099.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-1223T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423653 | |||||||
| chr17:58423775 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1721-1345C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423775 | |||||||
| chr17:58423893 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1721-1463G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423893 | |||||||
| chr17:58424051 | C | T | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-1621G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424051 | |||||||
| chr17:58424059 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1721-1629T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424059 | |||||||
| chr17:58424120 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1721-1690T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424120 | |||||||
| chr17:58424189 | ACAGCAGT others(5): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1721-1771_1721-176 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424189 | |||||||
| chr17:58424387 | CA | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1721-1958delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424387 | |||||||
| chr17:58424611 | C | CA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0096 a0001c0001t0001g0124 others(6): Show |
10 | HG01109.hp1 HG02451.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-2182dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424611 | |||||||
| chr17:58424611 | CA | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0274 a0001c0001t0001g0276 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-2182delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424611 | |||||||
| chr17:58424903 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(21): Show |
29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-2473G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424903 | |||||||
| chr17:58425406 | TA | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-2977delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425406 | |||||||
| chr17:58425575 | C | CA | 85 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(82): Show |
87 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1721-3146dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | |||||||
| chr17:58425575 | C | CAA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(13): Show |
19 | HG00544.hp1 HG00642.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.1721-3147_1721-314 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | |||||||
| chr17:58425575 | C | CAAAA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
16 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1721-3149_1721-314 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | |||||||
| chr17:58425575 | CA | C | 11 | a0001c0001t0001g0094 a0001c0001t0001g0156 a0001c0001t0001g0185 others(8): Show |
11 | HG01169.hp1 HG01255.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1721-3146delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | |||||||
| chr17:58425575 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-3155_1721-314 others(14): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | |||||||
| chr17:58425590 | A | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0085 others(10): Show |
13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-3160T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425590 | |||||||
| chr17:58425974 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1721-3544T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425974 | |||||||
| chr17:58426373 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1721-3943A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58426373 | |||||||
| chr17:58426973 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1721-4543G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58426973 | |||||||
| chr17:58427129 | T | C | 3 | a0001c0001t0001g0093 a0001c0005t0001g0069 a0001c0005t0001g0073 |
3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1721-4699A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427129 | |||||||
| chr17:58427292 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1721-4862T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427292 | |||||||
| chr17:58427512 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 |
6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-5082C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427512 | |||||||
| chr17:58427868 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1721-5438C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427868 | |||||||
| chr17:58427932 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5502G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427932 | |||||||
| chr17:58428165 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5735G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428165 | |||||||
| chr17:58428202 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1721-5772G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428202 | |||||||
| chr17:58428402 | G | GT | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5973dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428402 | |||||||
| chr17:58428444 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1721-6014C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428444 | |||||||
| chr17:58428448 | A | G | 1 | a0002c0002t0001g0266 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1721-6018T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428448 | |||||||
| chr17:58428590 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1721-6160G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428590 | |||||||
| chr17:58428602 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1721-6172A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428602 | |||||||
| chr17:58428752 | G | A | 1 | a0002c0002t0001g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1721-6322C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428752 | |||||||
| chr17:58428799 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
118 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1721-6369T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428799 | |||||||
| chr17:58428976 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-6546A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428976 | |||||||
| chr17:58429124 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1721-6694C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429124 | |||||||
| chr17:58429273 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-6843C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429273 | |||||||
| chr17:58429482 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1721-7052G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429482 | |||||||
| chr17:58429500 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1721-7070G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429500 | |||||||
| chr17:58429702 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
96 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1721-7272G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429702 | |||||||
| chr17:58429719 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1721-7289C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429719 | |||||||
| chr17:58429756 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1721-7326C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429756 | |||||||
| chr17:58429842 | T | TA | 67 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0052 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1721-7413dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | |||||||
| chr17:58429842 | T | TAAA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
22 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1721-7415_1721-741 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | |||||||
| chr17:58429842 | TA | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 |
6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-7413delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | |||||||
| chr17:58430058 | C | T | 3 | a0002c0002t0001g0051 a0002c0002t0001g0258 a0002c0002t0001g0266 |
3 | HG02071.hp1 NA18943.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1721-7628G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430058 | |||||||
| chr17:58430178 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0173 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1721-7748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430178 | |||||||
| chr17:58430584 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1721-8154C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430584 | |||||||
| chr17:58431055 | A | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-8625T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431055 | |||||||
| chr17:58431285 | G | T | 1 | a0002c0002t0001g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1721-8855C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431285 | |||||||
| chr17:58431412 | A | C | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
5 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1721-8982T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431412 | |||||||
| chr17:58431449 | T | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-9019A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431449 | |||||||
| chr17:58431547 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1721-9117C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431547 | |||||||
| chr17:58431602 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1721-9172T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431602 | |||||||
| chr17:58431608 | A | G | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-9178T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431608 | |||||||
| chr17:58432036 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0049 |
3 | NA18946.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1721-9606G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432036 | |||||||
| chr17:58432106 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1721-9676A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432106 | |||||||
| chr17:58432202 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1721-9772A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432202 | |||||||
| chr17:58432263 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1721-9833G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432263 | |||||||
| chr17:58432504 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(21): Show |
29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-10074G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432504 | |||||||
| chr17:58432779 | A | G | 66 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(63): Show |
69 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1721-10349T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432779 | |||||||
| chr17:58432898 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1721-10468A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432898 | |||||||
| chr17:58432944 | G | A | 56 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0051 others(53): Show |
58 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1721-10514C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432944 | |||||||
| chr17:58432998 | C | CCATT | 75 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(72): Show |
75 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1721-10572_1721-10 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | |||||||
| chr17:58432998 | C | CCATTCAT others(5): Show |
2 | a0001c0005t0001g0069 a0001c0005t0001g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1721-10580_1721-10 others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | |||||||
| chr17:58432998 | CCATT | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0064 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-10572_1721-10 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | |||||||
| chr17:58433426 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0211 |
2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1721-10996A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433426 | |||||||
| chr17:58433602 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1721-11172A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433602 | |||||||
| chr17:58433746 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-11316C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433746 | |||||||
| chr17:58433875 | A | G | 1 | a0002c0002t0001g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1721-11445T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433875 | |||||||
| chr17:58433911 | A | AT | 7 | a0001c0001t0001g0084 a0001c0001t0001g0096 a0001c0001t0001g0133 others(4): Show |
7 | HG00544.hp2 HG01981.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-11482dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | |||||||
| chr17:58433911 | A | ATTTTTTT others(1): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(24): Show |
31 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1721-11489_1721-11 others(14): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | |||||||
| chr17:58433911 | A | ATTTTTTT others(2): Show |
126 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1721-11490_1721-11 others(15): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | |||||||
| chr17:58433911 | A | ATTTTTTT others(3): Show |
38 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0044 others(35): Show |
39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1721-11491_1721-11 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | |||||||
| chr17:58433911 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0213 a0002c0002t0001g0221 |
3 | NA18994.hp2 NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1721-11492_1721-11 others(17): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | |||||||
| chr17:58433986 | T | TCAGTGCA others(5): Show |
1 | a0001c0001t0001g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1721-11568_1721-11 others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433986 | |||||||
| chr17:58434102 | G | A | 1 | a0008c0010t0001g0047 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1721-11672C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434102 | |||||||
| chr17:58434102 | G | T | 1 | a0001c0001t0001g0005 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1721-11672C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434102 | |||||||
| chr17:58434189 | A | G | 1 | a0002c0002t0001g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1721-11759T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434189 | |||||||
| chr17:58434300 | G | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-11870C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434300 | |||||||
| chr17:58434418 | G | A | 1 | a0002c0002t0001g0257 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1721-11988C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434418 | |||||||
| chr17:58434420 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1721-11990C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434420 | |||||||
| chr17:58434544 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-12114G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434544 | |||||||
| chr17:58434549 | CA | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0121 others(5): Show |
8 | HG00558.hp2 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1721-12120delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434549 | |||||||
| chr17:58434563 | A | G | 61 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(58): Show |
61 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1721-12133T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434563 | |||||||
| chr17:58434725 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1721-12295C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434725 | |||||||
| chr17:58434844 | C | T | 2 | a0002c0002t0001g0051 a0002c0002t0001g0258 |
2 | HG02071.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1721-12414G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434844 | |||||||
| chr17:58434875 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-12445A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434875 | |||||||
| chr17:58434956 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0161 a0001c0001t0001g0310 |
4 | NA18946.hp1 NA18993.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-12526A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434956 | |||||||
| chr17:58435264 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1721-12834A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435264 | |||||||
| chr17:58435270 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1721-12840C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435270 | |||||||
| chr17:58435741 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1721-13311A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435741 | |||||||
| chr17:58435758 | G | A | 1 | a0009c0008t0001g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1721-13328C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435758 | |||||||
| chr17:58435791 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-13361G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435791 | |||||||
| chr17:58435794 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0280 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-13364C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435794 | |||||||
| chr17:58435832 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-13402C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435832 | |||||||
| chr17:58435898 | C | CA | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(100): Show |
105 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1721-13469dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435898 | |||||||
| chr17:58436345 | CT | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(22): Show |
30 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1721-13916delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436345 | |||||||
| chr17:58436498 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00639.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1721-14068T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436498 | |||||||
| chr17:58436504 | T | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14074A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436504 | |||||||
| chr17:58436536 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14106A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436536 | |||||||
| chr17:58436735 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14305G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436735 | |||||||
| chr17:58436840 | T | C | 4 | a0002c0002t0001g0221 a0002c0002t0001g0256 a0002c0002t0001g0268 others(1): Show |
4 | NA18997.hp1 NA19064.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-14410A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436840 | |||||||
| chr17:58436840 | T | TAAC | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14413_1721-14 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436840 | |||||||
| chr17:58436932 | AC | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(95): Show |
99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1721-14503delG | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436932 | |||||||
| chr17:58437097 | G | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(95): Show |
99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1721-14667C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58437097 | |||||||
| chr17:58437927 | G | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0302 |
2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1721-15497C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58437927 | |||||||
| chr17:58438029 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1721-15599A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438029 | |||||||
| chr17:58438213 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1721-15783T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438213 | |||||||
| chr17:58438249 | C | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-15819G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438249 | |||||||
| chr17:58438358 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1721-15928T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438358 | |||||||
| chr17:58438671 | A | G | 1 | a0002c0002t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1721-16241T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438671 | |||||||
| chr17:58438814 | T | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(3): Show |
6 | HG00642.hp1 HG03704.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-16384A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438814 | |||||||
| chr17:58438816 | GCACTAAG others(6): Show |
G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(3): Show |
6 | HG00642.hp1 HG03704.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-16399_1721-16 others(19): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438816 | |||||||
| chr17:58438885 | G | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0097 |
5 | HG01884.hp1 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-16455C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438885 | |||||||
| chr17:58438894 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1721-16464T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438894 | |||||||
| chr17:58438976 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1721-16546T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438976 | |||||||
| chr17:58439126 | CA | C | 12 | a0002c0002t0001g0012 a0002c0002t0001g0169 a0002c0002t0001g0222 others(9): Show |
13 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1721-16697delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439126 | |||||||
| chr17:58439134 | A | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-16704T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439134 | |||||||
| chr17:58439275 | A | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-16845T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439275 | |||||||
| chr17:58439284 | A | AAAC | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(21): Show |
29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-16857_1721-16 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439284 | |||||||
| chr17:58439333 | ACATATGT others(11): Show |
A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1721-16921_1721-16 others(24): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439333 | |||||||
| chr17:58439447 | C | G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0191 a0001c0001t0001g0200 others(1): Show |
4 | NA18994.hp2 NA19001.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-17017G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439447 | |||||||
| chr17:58439471 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-17041T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439471 | |||||||
| chr17:58439506 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0207 |
2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1721-17076G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439506 | |||||||
| chr17:58439673 | G | A | 170 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0038 others(167): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1721-17243C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439673 | |||||||
| chr17:58439727 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-17297C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439727 | |||||||
| chr17:58440130 | G | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-17700C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440130 | |||||||
| chr17:58440417 | T | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0188 a0001c0001t0001g0214 others(2): Show |
5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-17987A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440417 | |||||||
| chr17:58440601 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1720+18167C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440601 | |||||||
| chr17:58440767 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+18001G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440767 | |||||||
| chr17:58440937 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1720+17831C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440937 | |||||||
| chr17:58440940 | T | TA | 19 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+17827dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440940 | |||||||
| chr17:58441015 | CAGAT | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+17749_1720+17 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441015 | |||||||
| chr17:58441173 | T | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0001g0208 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+17595A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441173 | |||||||
| chr17:58441844 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1720+16924C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441844 | |||||||
| chr17:58442130 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1720+16638C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442130 | |||||||
| chr17:58442267 | C | G | 1 | a0007c0006t0001g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1720+16501G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442267 | |||||||
| chr17:58442379 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1720+16389C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442379 | |||||||
| chr17:58442675 | C | A | 67 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1720+16093G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442675 | |||||||
| chr17:58442713 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+16055T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442713 | |||||||
| chr17:58442716 | CTTAG | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0280 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+16048_1720+16 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442716 | |||||||
| chr17:58442766 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1720+16002A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442766 | |||||||
| chr17:58442789 | G | A | 1 | a0002c0002t0001g0268 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1720+15979C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442789 | |||||||
| chr17:58442862 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0292 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1720+15906A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442862 | |||||||
| chr17:58442873 | G | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+15895C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442873 | |||||||
| chr17:58442912 | A | AT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(21): Show |
28 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1720+15855dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442912 | |||||||
| chr17:58442987 | C | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+15781G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442987 | |||||||
| chr17:58443065 | G | A | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
117 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1720+15703C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443065 | |||||||
| chr17:58443098 | G | A | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+15670C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443098 | |||||||
| chr17:58443164 | C | A | 3 | a0002c0002t0001g0012 a0002c0002t0001g0169 a0002c0002t0001g0245 |
4 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+15604G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443164 | |||||||
| chr17:58443227 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1720+15541G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443227 | |||||||
| chr17:58443234 | T | C | 7 | a0002c0002t0001g0233 a0002c0002t0001g0237 a0002c0002t0001g0241 others(4): Show |
7 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+15534A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443234 | |||||||
| chr17:58443284 | A | AGT | 5 | a0001c0001t0001g0183 a0001c0001t0001g0188 a0001c0001t0001g0214 others(2): Show |
5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+15483_1720+15 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443284 | |||||||
| chr17:58443737 | C | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+15031G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443737 | |||||||
| chr17:58443768 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
16 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1720+15000G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443768 | |||||||
| chr17:58443828 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1720+14940A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443828 | |||||||
| chr17:58443882 | G | A | 3 | a0002c0002t0001g0224 a0002c0002t0001g0257 a0002c0002t0001g0259 |
3 | NA18612.hp2 NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1720+14886C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443882 | |||||||
| chr17:58443927 | G | A | 1 | a0002c0002t0001g0227 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1720+14841C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443927 | |||||||
| chr17:58443946 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1720+14822C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443946 | |||||||
| chr17:58444023 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14745G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444023 | |||||||
| chr17:58444030 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1720+14738C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444030 | |||||||
| chr17:58444097 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1720+14671A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444097 | |||||||
| chr17:58444498 | GA | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14269delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444498 | |||||||
| chr17:58444649 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14119A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444649 | |||||||
| chr17:58444657 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1720+14111G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444657 | |||||||
| chr17:58444676 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14092C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444676 | |||||||
| chr17:58445022 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1720+13746T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445022 | |||||||
| chr17:58445082 | C | T | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+13686G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445082 | |||||||
| chr17:58445172 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1720+13596T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445172 | |||||||
| chr17:58445474 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1720+13294A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445474 | |||||||
| chr17:58445618 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+13150A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445618 | |||||||
| chr17:58445721 | G | C | 5 | a0002c0002t0001g0062 a0002c0002t0001g0234 a0002c0002t0001g0239 others(2): Show |
5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+13047C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445721 | |||||||
| chr17:58445816 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0260 others(5): Show |
9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+12952T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445816 | |||||||
| chr17:58445927 | G | A | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+12841C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445927 | |||||||
| chr17:58445942 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+12826G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445942 | |||||||
| chr17:58446137 | C | CA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0176 others(9): Show |
14 | HG00438.hp2 HG01175.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+12630dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446137 | |||||||
| chr17:58446137 | CA | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0177 others(3): Show |
6 | HG01256.hp2 HG01515.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+12630delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446137 | |||||||
| chr17:58446157 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+12611C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446157 | |||||||
| chr17:58446158 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1720+12610C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446158 | |||||||
| chr17:58446186 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+12582G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446186 | |||||||
| chr17:58446288 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+12480G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446288 | |||||||
| chr17:58446433 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1720+12335A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446433 | |||||||
| chr17:58446442 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+12326A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446442 | |||||||
| chr17:58446539 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+12229C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446539 | |||||||
| chr17:58446644 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0001g0208 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+12124C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446644 | |||||||
| chr17:58446849 | A | G | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+11919T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446849 | |||||||
| chr17:58446941 | A | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+11827T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446941 | |||||||
| chr17:58446945 | T | C | 86 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(83): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1720+11823A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446945 | |||||||
| chr17:58447040 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+11728C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447040 | |||||||
| chr17:58447070 | AGCCAAGA others(4): Show |
A | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+11687_1720+11 others(17): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447070 | |||||||
| chr17:58447368 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1720+11400C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447368 | |||||||
| chr17:58447620 | G | A | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+11148C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447620 | |||||||
| chr17:58448078 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+10690C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448078 | |||||||
| chr17:58448133 | C | CA | 18 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0080 others(15): Show |
18 | HG01070.hp1 HG01081.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1720+10634dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | |||||||
| chr17:58448133 | CA | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1720+10634delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | |||||||
| chr17:58448133 | CAA | C | 79 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(76): Show |
79 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1720+10633_1720+10 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | |||||||
| chr17:58448375 | T | G | 1 | a0002c0002t0001g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1720+10393A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448375 | |||||||
| chr17:58448428 | A | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+10340T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448428 | |||||||
| chr17:58448705 | C | T | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+10063G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448705 | |||||||
| chr17:58448735 | GCAA | G | 23 | a0002c0002t0001g0062 a0002c0002t0001g0187 a0002c0002t0001g0233 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1720+10030_1720+10 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448735 | |||||||
| chr17:58448791 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1720+9977T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448791 | |||||||
| chr17:58449466 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+9302C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449466 | |||||||
| chr17:58449689 | G | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0188 a0001c0001t0001g0214 others(2): Show |
5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+9079C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449689 | |||||||
| chr17:58449697 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1720+9071G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449697 | |||||||
| chr17:58449699 | CA | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
105 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1720+9068delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449699 | |||||||
| chr17:58449715 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 others(1): Show |
8 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1720+9053T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449715 | |||||||
| chr17:58449751 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1720+9017G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449751 | |||||||
| chr17:58449756 | G | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1720+9012C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449756 | |||||||
| chr17:58449795 | G | A | 1 | a0001c0001t0010g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1720+8973C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449795 | |||||||
| chr17:58449820 | G | A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(93): Show |
97 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1720+8948C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449820 | |||||||
| chr17:58449839 | C | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0001g0208 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+8929G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449839 | |||||||
| chr17:58449939 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1720+8829G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449939 | |||||||
| chr17:58449954 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 |
6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+8814G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449954 | |||||||
| chr17:58450022 | C | CA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(30): Show |
34 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1720+8745dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450022 | |||||||
| chr17:58450022 | CAAAAAAA others(1): Show |
C | 65 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(62): Show |
68 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1720+8738_1720+874 others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450022 | |||||||
| chr17:58450208 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+8560C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450208 | |||||||
| chr17:58450261 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0153 |
3 | HG02004.hp1 HG02273.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1720+8507G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450261 | |||||||
| chr17:58450295 | CGCCATTG others(3249): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1720+5217_1720+847 others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450295 | |||||||
| chr17:58450337 | T | C | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+8431A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450337 | |||||||
| chr17:58450338 | C | CA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0038 others(17): Show |
22 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.1720+8429dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450338 | |||||||
| chr17:58450338 | CA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1720+8429delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450338 | |||||||
| chr17:58450443 | A | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+8325T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450443 | |||||||
| chr17:58450644 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+8124A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450644 | |||||||
| chr17:58450740 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0300 |
5 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+8028G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450740 | |||||||
| chr17:58450753 | C | CA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1720+8014dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450753 | |||||||
| chr17:58450994 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1720+7774G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450994 | |||||||
| chr17:58451003 | C | T | 1 | a0005c0009t0001g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1720+7765G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451003 | |||||||
| chr17:58451106 | T | C | 26 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0169 others(23): Show |
27 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1720+7662A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451106 | |||||||
| chr17:58451109 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0260 others(5): Show |
9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+7659G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451109 | |||||||
| chr17:58451536 | C | T | 1 | a0002c0002t0001g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1720+7232G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451536 | |||||||
| chr17:58451600 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1720+7168C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451600 | |||||||
| chr17:58451819 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1720+6949T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451819 | |||||||
| chr17:58451948 | T | TA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1720+6819dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451948 | |||||||
| chr17:58451948 | T | TAA | 92 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(89): Show |
93 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1720+6818_1720+681 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451948 | |||||||
| chr17:58451973 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+6795G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451973 | |||||||
| chr17:58452092 | T | A | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6676A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452092 | |||||||
| chr17:58452138 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6630T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452138 | |||||||
| chr17:58452198 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+6570A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452198 | |||||||
| chr17:58452412 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1720+6356A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452412 | |||||||
| chr17:58452480 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1720+6288G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452480 | |||||||
| chr17:58452622 | C | G | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6146G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452622 | |||||||
| chr17:58452738 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+6030C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452738 | |||||||
| chr17:58452875 | TA | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1720+5892delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452875 | |||||||
| chr17:58453236 | C | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(25): Show |
33 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1720+5532G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453236 | |||||||
| chr17:58453386 | G | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+5382C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453386 | |||||||
| chr17:58453576 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1720+5192G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453576 | |||||||
| chr17:58453599 | A | AAAC | 19 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0057 others(16): Show |
19 | HG00544.hp2 HG01255.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1720+5166_1720+516 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | |||||||
| chr17:58453599 | A | AAACAAC | 19 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
20 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+5163_1720+516 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | |||||||
| chr17:58453599 | AAAC | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0003c0003t0001g0015 others(1): Show |
7 | HG01257.hp1 HG01258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+5166_1720+516 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | |||||||
| chr17:58453707 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+5061T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453707 | |||||||
| chr17:58453880 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0292 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1720+4888C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453880 | |||||||
| chr17:58453916 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1720+4852C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453916 | |||||||
| chr17:58453952 | G | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(94): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1720+4816C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453952 | |||||||
| chr17:58453964 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1720+4804G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453964 | |||||||
| chr17:58454241 | A | C | 2 | a0001c0001t0003g0098 a0001c0001t0003g0301 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1720+4527T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454241 | |||||||
| chr17:58454258 | A | T | 1 | a0006c0011t0001g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1720+4510T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454258 | |||||||
| chr17:58454833 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1720+3935T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454833 | |||||||
| chr17:58455049 | A | G | 1 | a0005c0009t0001g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1720+3719T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455049 | |||||||
| chr17:58455327 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+3441G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455327 | |||||||
| chr17:58455397 | G | C | 1 | a0004c0007t0001g0195 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1720+3371C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455397 | |||||||
| chr17:58455418 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1720+3350G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455418 | |||||||
| chr17:58455536 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1720+3232T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455536 | |||||||
| chr17:58455596 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1720+3172G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455596 | |||||||
| chr17:58455709 | A | C | 1 | a0002c0002t0001g0250 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1720+3059T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455709 | |||||||
| chr17:58455874 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1720+2894C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455874 | |||||||
| chr17:58455926 | G | T | 1 | a0002c0002t0001g0236 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1720+2842C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455926 | |||||||
| chr17:58455927 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1720+2841A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455927 | |||||||
| chr17:58456127 | ATATG | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+2637_1720+264 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456127 | |||||||
| chr17:58456129 | A | G | 2 | a0001c0005t0001g0069 a0001c0005t0001g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1720+2639T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456129 | |||||||
| chr17:58456141 | A | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0001g0208 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+2627T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456141 | |||||||
| chr17:58456151 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0174 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1720+2617T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456151 | |||||||
| chr17:58456153 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0181 others(7): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+2615C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456153 | |||||||
| chr17:58456161 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0174 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1720+2607C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456161 | |||||||
| chr17:58456161 | GTA | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0057 others(9): Show |
13 | HG01243.hp2 HG02257.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1720+2605_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456161 | |||||||
| chr17:58456163 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0274 others(5): Show |
10 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1720+2605T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456163 | |||||||
| chr17:58456164 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0174 a0001c0001t0001g0275 |
3 | HG02559.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1720+2604A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | |||||||
| chr17:58456164 | T | TAC | 67 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(64): Show |
67 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1720+2603_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | |||||||
| chr17:58456164 | TATAC | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0075 others(3): Show |
6 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | |||||||
| chr17:58456166 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1720+2602A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456166 | T | TAC | 11 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0104 others(8): Show |
12 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456166 | T | TACACAC | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0311 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+2596_1720+260 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456166 | TAC | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0052 others(55): Show |
62 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456166 | TACAC | T | 3 | a0001c0001t0001g0261 a0002c0002t0001g0247 a0002c0002t0001g0258 |
3 | HG02071.hp1 HG02135.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1720+2598_1720+260 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456166 | TACACACA others(5): Show |
T | 1 | a0001c0001t0010g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1720+2590_1720+260 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | |||||||
| chr17:58456168 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1720+2600G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456168 | |||||||
| chr17:58456199 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+2569C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456199 | |||||||
| chr17:58456433 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1720+2335C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456433 | |||||||
| chr17:58456644 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+2124A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456644 | |||||||
| chr17:58456803 | T | G | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+1965A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456803 | |||||||
| chr17:58456895 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+1873C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456895 | |||||||
| chr17:58457048 | CA | C | 67 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1720+1719delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457048 | |||||||
| chr17:58457269 | A | T | 4 | a0001c0001t0001g0152 a0002c0002t0001g0011 a0002c0002t0001g0248 others(1): Show |
5 | HG01496.hp1 NA18945.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+1499T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457269 | |||||||
| chr17:58457272 | T | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0059 others(5): Show |
10 | HG01192.hp2 HG01243.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1720+1496A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457272 | |||||||
| chr17:58457424 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1720+1344G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457424 | |||||||
| chr17:58458005 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0280 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1720+763G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458005 | |||||||
| chr17:58458328 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1720+440G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458328 | |||||||
| chr17:58458571 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1720+197T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458571 | |||||||
| chr17:58458606 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1720+162T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458606 | |||||||
| chr17:58458661 | C | T | 1 | a0002c0002t0001g0248 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1720+107G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458661 | |||||||
| chr17:58459166 | T | C | 1 | a0001c0001t0003g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1543-221A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459166 | |||||||
| chr17:58459646 | C | CA | 87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(84): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1543-702dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459646 | |||||||
| chr17:58459664 | G | T | 2 | a0002c0002t0001g0234 a0002c0002t0001g0236 |
2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1543-719C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459664 | |||||||
| chr17:58459740 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 |
6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-795C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459740 | |||||||
| chr17:58459848 | C | G | 1 | a0001c0001t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1543-903G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459848 | |||||||
| chr17:58460212 | TCTCA | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-1271_1543-126 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460212 | |||||||
| chr17:58460354 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
5 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-1409C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460354 | |||||||
| chr17:58460374 | A | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1543-1429T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460374 | |||||||
| chr17:58460470 | C | CAT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG01243.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-1527_1543-152 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460470 | |||||||
| chr17:58460470 | CAT | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(9): Show |
13 | HG00741.hp1 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1543-1527_1543-152 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460470 | |||||||
| chr17:58460476 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0092 a0002c0002t0001g0051 others(7): Show |
10 | HG00323.hp1 HG02071.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543-1531A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460476 | |||||||
| chr17:58460478 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1543-1533A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460478 | |||||||
| chr17:58460510 | C | CACACACA others(1): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0038 others(5): Show |
8 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | |||||||
| chr17:58460510 | C | CACACAT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(29): Show |
34 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | |||||||
| chr17:58460510 | C | CACAT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0032 others(81): Show |
87 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | |||||||
| chr17:58460510 | C | CAT | 103 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(100): Show |
108 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1543-1567_1543-156 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | |||||||
| chr17:58460510 | C | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0049 others(76): Show |
84 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1543-1565G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | |||||||
| chr17:58460514 | C | A | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-1569G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460514 | |||||||
| chr17:58460515 | T | C | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-1570A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460515 | |||||||
| chr17:58460715 | TAA | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1543-1772_1543-177 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460715 | |||||||
| chr17:58460755 | C | T | 2 | a0001c0005t0001g0069 a0001c0005t0001g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1543-1810G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460755 | |||||||
| chr17:58461189 | G | A | 1 | a0001c0001t0006g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1542+1593C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461189 | |||||||
| chr17:58461202 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542+1580T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461202 | |||||||
| chr17:58461213 | CACA | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(10): Show |
14 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1542+1566_1542+156 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461213 | CACAACA | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
187 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.1542+1563_1542+156 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461213 | CACAACAA others(2): Show |
C | 80 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0078 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1542+1560_1542+156 others(13): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461213 | CACAACAA others(5): Show |
C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(16): Show |
22 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1542+1557_1542+156 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461213 | CACAACAA others(8): Show |
C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(4): Show |
8 | HG00323.hp2 HG01074.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+1554_1542+156 others(19): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461213 | CACAACAA others(11): Show |
C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
16 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542+1551_1542+156 others(22): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | |||||||
| chr17:58461278 | T | C | 67 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1542+1504A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461278 | |||||||
| chr17:58461284 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+1498C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461284 | |||||||
| chr17:58461469 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1542+1313G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461469 | |||||||
| chr17:58461493 | G | A | 1 | a0002c0002t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1542+1289C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461493 | |||||||
| chr17:58461512 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1542+1270A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461512 | |||||||
| chr17:58461647 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1542+1135C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461647 | |||||||
| chr17:58461737 | T | C | 2 | a0002c0002t0001g0187 a0006c0011t0001g0226 |
2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1542+1045A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461737 | |||||||
| chr17:58461743 | G | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG01168.hp2 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+1039C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461743 | |||||||
| chr17:58461828 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1542+954G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461828 | |||||||
| chr17:58461922 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1542+860G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461922 | |||||||
| chr17:58462127 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1542+655G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462127 | |||||||
| chr17:58462127 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1542+655G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462127 | |||||||
| chr17:58462131 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542+651G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462131 | |||||||
| chr17:58462431 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542+351A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462431 | |||||||
| chr17:58462469 | A | C | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1542+313T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462469 | |||||||
| chr17:58462529 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1542+253G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462529 | |||||||
| chr17:58462636 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1542+146T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462636 | |||||||
| chr17:58462749 | G | A | 67 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1542+33C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462749 | |||||||
| chr17:58463733 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1021-430G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463733 | |||||||
| chr17:58463753 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1021-450C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463753 | |||||||
| chr17:58463891 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1021-588T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463891 | |||||||
| chr17:58464082 | TA | T | 86 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(83): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1021-780delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464082 | |||||||
| chr17:58464434 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1021-1131C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464434 | |||||||
| chr17:58464486 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0164 |
2 | NA18998.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1021-1183G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464486 | |||||||
| chr17:58464823 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1021-1520C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464823 | |||||||
| chr17:58464823 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1021-1520C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464823 | |||||||
| chr17:58464903 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1021-1600A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464903 | |||||||
| chr17:58465177 | CTTTTCTT others(5): Show |
C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(7): Show |
11 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+1696_1020+170 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465177 | |||||||
| chr17:58465182 | C | CT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0281 others(49): Show |
55 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1020+1702dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465182 | |||||||
| chr17:58465182 | CT | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0037 others(12): Show |
15 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1020+1702delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465182 | |||||||
| chr17:58465252 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1020+1633G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465252 | |||||||
| chr17:58465604 | C | G | 2 | a0001c0005t0001g0069 a0001c0005t0001g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1020+1281G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465604 | |||||||
| chr17:58465615 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1020+1270C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465615 | |||||||
| chr17:58465624 | CA | C | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1020+1260delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465624 | |||||||
| chr17:58465638 | A | G | 1 | a0001c0001t0010g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1020+1247T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465638 | |||||||
| chr17:58465824 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1020+1061C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465824 | |||||||
| chr17:58465831 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1020+1054A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465831 | |||||||
| chr17:58465956 | C | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0211 |
2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1020+929G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465956 | |||||||
| chr17:58465979 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1020+906T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465979 | |||||||
| chr17:58466063 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1020+822A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466063 | |||||||
| chr17:58466076 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1020+809A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466076 | |||||||
| chr17:58466189 | C | T | 3 | a0002c0002t0001g0012 a0002c0002t0001g0169 a0002c0002t0001g0245 |
4 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+696G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466189 | |||||||
| chr17:58466359 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1020+526G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466359 | |||||||
| chr17:58466370 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0106 |
3 | HG01168.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1020+515G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466370 | |||||||
| chr17:58466465 | T | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0085 others(10): Show |
13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1020+420A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466465 | |||||||
| chr17:58466715 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1020+170A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466715 | |||||||
| chr17:58466726 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1020+159T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466726 | |||||||
| chr17:58466823 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1020+62A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466823 | |||||||
| chr17:58467013 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.926-34G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467013 | |||||||
| chr17:58467069 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.926-90A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467069 | |||||||
| chr17:58467424 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0005g0002 |
6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.926-445G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467424 | |||||||
| chr17:58467687 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.926-708A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467687 | |||||||
| chr17:58467708 | T | G | 290 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(287): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.926-729A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467708 | |||||||
| chr17:58467908 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-929G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467908 | |||||||
| chr17:58467983 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.926-1004G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467983 | |||||||
| chr17:58468039 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0292 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.926-1060G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468039 | |||||||
| chr17:58468094 | G | T | 1 | a0002c0002t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.926-1115C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468094 | |||||||
| chr17:58468116 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.926-1137T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468116 | |||||||
| chr17:58468469 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-1490A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468469 | |||||||
| chr17:58468556 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.926-1577T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468556 | |||||||
| chr17:58468859 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.926-1880C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468859 | |||||||
| chr17:58469098 | G | GA | 77 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0025 others(74): Show |
80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.926-2120dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469098 | |||||||
| chr17:58469138 | A | T | 2 | a0001c0005t0001g0069 a0001c0005t0001g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.926-2159T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469138 | |||||||
| chr17:58469163 | A | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.926-2184T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469163 | |||||||
| chr17:58469364 | T | A | 86 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(83): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.926-2385A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469364 | |||||||
| chr17:58469842 | T | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-2863A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469842 | |||||||
| chr17:58469848 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.926-2869A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469848 | |||||||
| chr17:58470019 | A | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-3040T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470019 | |||||||
| chr17:58470024 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0207 |
2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.926-3045C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470024 | |||||||
| chr17:58470042 | C | A | 26 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0169 others(23): Show |
27 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.926-3063G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470042 | |||||||
| chr17:58470176 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.926-3197G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470176 | |||||||
| chr17:58470798 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.926-3819G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470798 | |||||||
| chr17:58470920 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.926-3941G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470920 | |||||||
| chr17:58471059 | T | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
128 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.926-4080A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471059 | |||||||
| chr17:58471106 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.926-4127C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471106 | |||||||
| chr17:58471397 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.926-4418C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471397 | |||||||
| chr17:58471439 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4460C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471439 | |||||||
| chr17:58471450 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.926-4471T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471450 | |||||||
| chr17:58471556 | AT | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 others(1): Show |
4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-4578delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471556 | |||||||
| chr17:58471621 | C | CT | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.926-4643dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471621 | |||||||
| chr17:58471638 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.926-4659G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471638 | |||||||
| chr17:58471787 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.926-4808C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471787 | |||||||
| chr17:58471796 | G | C | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.926-4817C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471796 | |||||||
| chr17:58471844 | G | C | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.926-4865C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471844 | |||||||
| chr17:58471879 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4900C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471879 | |||||||
| chr17:58471901 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4922C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471901 | |||||||
| chr17:58471946 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.926-4967G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471946 | |||||||
| chr17:58472309 | C | A | 2 | a0001c0001t0004g0194 a0001c0001t0004g0210 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.926-5330G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472309 | |||||||
| chr17:58472310 | C | A | 86 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(83): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.926-5331G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472310 | |||||||
| chr17:58472311 | A | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(93): Show |
97 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.926-5332T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472311 | |||||||
| chr17:58472647 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.926-5668A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472647 | |||||||
| chr17:58472926 | T | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-5947A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472926 | |||||||
| chr17:58472939 | C | T | 67 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0246 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.926-5960G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472939 | |||||||
| chr17:58473052 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.926-6073C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473052 | |||||||
| chr17:58473074 | C | G | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.926-6095G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473074 | |||||||
| chr17:58473165 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.926-6186T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473165 | |||||||
| chr17:58473327 | T | G | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-6348A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473327 | |||||||
| chr17:58473443 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
128 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.925+6450A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473443 | |||||||
| chr17:58473591 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.925+6302C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473591 | |||||||
| chr17:58473778 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.925+6115T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473778 | |||||||
| chr17:58473896 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.925+5997G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473896 | |||||||
| chr17:58473931 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0260 a0001c0001t0001g0261 |
4 | HG02622.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+5962T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473931 | |||||||
| chr17:58473932 | A | G | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+5961T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473932 | |||||||
| chr17:58473954 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925+5939A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473954 | |||||||
| chr17:58474096 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+5797C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474096 | |||||||
| chr17:58474389 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.925+5504G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474389 | |||||||
| chr17:58474464 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.925+5429A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474464 | |||||||
| chr17:58474473 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.925+5420A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474473 | |||||||
| chr17:58474524 | T | C | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.925+5369A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474524 | |||||||
| chr17:58474691 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.925+5202C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474691 | |||||||
| chr17:58474827 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0125 a0001c0001t0001g0152 |
3 | HG01496.hp1 HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.925+5066G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474827 | |||||||
| chr17:58474843 | A | G | 292 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.925+5050T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474843 | |||||||
| chr17:58474992 | A | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(93): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.925+4901T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474992 | |||||||
| chr17:58475042 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+4851G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475042 | |||||||
| chr17:58475145 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.925+4748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475145 | |||||||
| chr17:58475541 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.925+4352T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475541 | |||||||
| chr17:58475692 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.925+4201C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475692 | |||||||
| chr17:58475899 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.925+3994T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475899 | |||||||
| chr17:58476227 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+3666G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476227 | |||||||
| chr17:58476235 | C | CTCTTCAT others(20): Show |
1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+3631_925+3657d others(29): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476235 | |||||||
| chr17:58476324 | T | G | 1 | a0003c0003t0008g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+3569A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476324 | |||||||
| chr17:58476347 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.925+3546C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476347 | |||||||
| chr17:58476770 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.925+3123T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476770 | |||||||
| chr17:58476868 | G | GT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG02602.hp1 HG02738.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+3024dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476868 | |||||||
| chr17:58476996 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.925+2897T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476996 | |||||||
| chr17:58477115 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+2778T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477115 | |||||||
| chr17:58477116 | C | CT | 17 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(14): Show |
18 | HG00438.hp2 HG01261.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.925+2776dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477116 | |||||||
| chr17:58477116 | CT | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0048 others(13): Show |
19 | HG00558.hp1 HG01243.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+2776delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477116 | |||||||
| chr17:58477129 | T | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
125 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.925+2764A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477129 | |||||||
| chr17:58477129 | T | TC | 3 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0132 |
3 | NA18949.hp2 NA18990.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.925+2763_925+2764i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477129 | |||||||
| chr17:58477150 | T | C | 1 | a0002c0002t0001g0243 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.925+2743A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477150 | |||||||
| chr17:58477173 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.925+2720C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477173 | |||||||
| chr17:58477181 | G | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.925+2712C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477181 | |||||||
| chr17:58477341 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.925+2552G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477341 | |||||||
| chr17:58477362 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0193 |
2 | HG00438.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.925+2531G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477362 | |||||||
| chr17:58477374 | C | T | 1 | a0001c0001t0010g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.925+2519G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477374 | |||||||
| chr17:58477426 | T | A | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+2467A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477426 | |||||||
| chr17:58477462 | CT | C | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.925+2430delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477462 | |||||||
| chr17:58477464 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0005g0002 a0002c0002t0001g0236 |
4 | HG00639.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+2429A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477464 | |||||||
| chr17:58477520 | C | T | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+2373G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477520 | |||||||
| chr17:58477523 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.925+2370C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477523 | |||||||
| chr17:58477545 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.925+2348G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477545 | |||||||
| chr17:58477592 | T | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0232 |
2 | NA18991.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.925+2301A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477592 | |||||||
| chr17:58477627 | T | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
128 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.925+2266A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477627 | |||||||
| chr17:58477667 | A | G | 1 | a0002c0002t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.925+2226T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477667 | |||||||
| chr17:58477682 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG01243.hp2 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+2211C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477682 | |||||||
| chr17:58477688 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
128 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.925+2205G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477688 | |||||||
| chr17:58477693 | C | G | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.925+2200G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477693 | |||||||
| chr17:58477726 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.925+2167A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477726 | |||||||
| chr17:58477986 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.925+1907A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477986 | |||||||
| chr17:58478171 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.925+1722G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478171 | |||||||
| chr17:58478270 | A | AAAAT | 80 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(77): Show |
83 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.925+1619_925+1622d others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478270 | |||||||
| chr17:58478280 | A | AAT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0061 |
5 | HG01106.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+1611_925+1612d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478280 | |||||||
| chr17:58478280 | A | AATAAAT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(42): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.925+1612_925+1613i others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478280 | |||||||
| chr17:58478282 | T | TAA | 162 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0038 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.925+1610_925+1611i others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478282 | |||||||
| chr17:58478284 | T | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0102 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+1609A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478284 | |||||||
| chr17:58478300 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0150 |
2 | HG04228.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925+1593A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478300 | |||||||
| chr17:58478302 | C | T | 105 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0056 others(102): Show |
109 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.925+1591G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478302 | |||||||
| chr17:58478353 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.925+1540A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478353 | |||||||
| chr17:58478384 | G | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(92): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.925+1509C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478384 | |||||||
| chr17:58478475 | C | CA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0108 others(3): Show |
7 | HG00621.hp2 HG01081.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+1417dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478475 | |||||||
| chr17:58478486 | AAAAAG | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0052 others(10): Show |
14 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.925+1402_925+1406d others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478486 | |||||||
| chr17:58478486 | AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0173 others(1): Show |
4 | HG02965.hp1 HG02976.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+1397_925+1406d others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478486 | |||||||
| chr17:58478539 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0206 |
2 | NA19011.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.925+1354A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478539 | |||||||
| chr17:58478864 | CA | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(168): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.925+1028delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478864 | |||||||
| chr17:58478960 | G | A | 1 | a0001c0001t0005g0002 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+933C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478960 | |||||||
| chr17:58479129 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.925+764T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479129 | |||||||
| chr17:58479287 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.925+606C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479287 | |||||||
| chr17:58479508 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.925+385C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479508 | |||||||
| chr17:58479601 | C | T | 2 | a0001c0001t0005g0002 a0001c0001t0010g0017 |
3 | HG02257.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+292G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479601 | |||||||
| chr17:58480400 | AAAC | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.551-136_551-134del others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480400 | |||||||
| chr17:58480476 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.551-209C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480476 | |||||||
| chr17:58480700 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.551-433G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480700 | |||||||
| chr17:58480762 | G | GCTAT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(109): Show |
116 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.551-499_551-496dup others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | |||||||
| chr17:58480762 | G | GCTATCTA others(1): Show |
83 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(80): Show |
87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.551-503_551-496dup others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | |||||||
| chr17:58480762 | G | GCTATCTA others(5): Show |
51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(48): Show |
55 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.551-507_551-496dup others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | |||||||
| chr17:58480762 | G | GCTATCTA others(9): Show |
13 | a0001c0001t0001g0034 a0001c0001t0001g0112 a0001c0001t0001g0121 others(10): Show |
13 | HG01358.hp1 HG02148.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.551-511_551-496dup others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | |||||||
| chr17:58480762 | GCTATCTA others(5): Show |
G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-507_551-496del others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | |||||||
| chr17:58480880 | C | T | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.551-613G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480880 | |||||||
| chr17:58481155 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.551-888A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481155 | |||||||
| chr17:58481238 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.551-971G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481238 | |||||||
| chr17:58481334 | T | C | 1 | a0006c0011t0001g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.551-1067A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481334 | |||||||
| chr17:58481557 | G | A | 291 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.551-1290C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481557 | |||||||
| chr17:58481644 | T | C | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.551-1377A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481644 | |||||||
| chr17:58481814 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.551-1547T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481814 | |||||||
| chr17:58482120 | T | TAAAC | 292 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.551-1854_551-1853i others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482120 | |||||||
| chr17:58482526 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0299 |
3 | HG00642.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.551-2259A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482526 | |||||||
| chr17:58482709 | C | CA | 59 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0031 others(56): Show |
59 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.551-2443dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482709 | C | CAA | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
85 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.551-2444_551-2443d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482709 | C | CAAA | 16 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0071 others(13): Show |
16 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.551-2445_551-2443d others(5): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482709 | CA | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(6): Show |
11 | HG01515.hp1 HG01515.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.551-2443delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482709 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.551-2452_551-2443d others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482709 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | NA18979.hp1 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.551-2458_551-2443d others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | |||||||
| chr17:58482837 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.551-2570C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482837 | |||||||
| chr17:58482940 | T | TA | 4 | a0001c0001t0001g0289 a0002c0002t0001g0051 a0002c0002t0001g0273 others(1): Show |
4 | HG02055.hp1 HG04115.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2674_551-2673i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482940 | |||||||
| chr17:58482941 | T | A | 67 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0225 others(64): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.551-2674A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482941 | |||||||
| chr17:58482941 | TA | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0061 others(18): Show |
23 | HG01069.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.551-2675delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482941 | |||||||
| chr17:58482997 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.551-2730C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482997 | |||||||
| chr17:58483015 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | NA18979.hp1 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.551-2748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483015 | |||||||
| chr17:58483116 | A | AT | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.551-2850_551-2849i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483116 | |||||||
| chr17:58483480 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-3213T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483480 | |||||||
| chr17:58483499 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-3232A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483499 | |||||||
| chr17:58484117 | A | T | 1 | a0002c0002t0001g0286 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.550+3608T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484117 | |||||||
| chr17:58484205 | G | GA | 12 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0108 others(9): Show |
12 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.550+3519dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484205 | |||||||
| chr17:58484581 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.550+3144G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484581 | |||||||
| chr17:58484591 | GA | G | 87 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(84): Show |
87 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.550+3133delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484591 | |||||||
| chr17:58484701 | G | A | 290 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(287): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.550+3024C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484701 | |||||||
| chr17:58484771 | C | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(95): Show |
99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.550+2954G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484771 | |||||||
| chr17:58484924 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.550+2801T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484924 | |||||||
| chr17:58484945 | AT | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0025 others(48): Show |
52 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.550+2779delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | |||||||
| chr17:58484945 | ATT | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(106): Show |
115 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.550+2778_550+2779d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | |||||||
| chr17:58484945 | ATTT | A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
147 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.550+2777_550+2779d others(5): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | |||||||
| chr17:58485103 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.550+2622G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485103 | |||||||
| chr17:58485174 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00558.hp2 NA18747.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.550+2551G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485174 | |||||||
| chr17:58485312 | T | C | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+2413A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485312 | |||||||
| chr17:58485348 | T | A | 2 | a0002c0002t0001g0278 a0002c0002t0001g0279 |
2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.550+2377A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485348 | |||||||
| chr17:58485435 | G | A | 2 | a0001c0004t0001g0167 a0001c0004t0001g0313 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.550+2290C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485435 | |||||||
| chr17:58485619 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.550+2106G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485619 | |||||||
| chr17:58485690 | T | G | 2 | a0002c0002t0001g0290 a0002c0002t0001g0291 |
2 | NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.550+2035A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485690 | |||||||
| chr17:58485728 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.550+1997G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485728 | |||||||
| chr17:58485746 | C | CA | 145 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(142): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.550+1978dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | |||||||
| chr17:58485746 | C | CAA | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00438.hp1 HG02055.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.550+1977_550+1978d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | |||||||
| chr17:58485746 | CA | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0295 others(3): Show |
7 | HG00323.hp1 HG01099.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1978delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | |||||||
| chr17:58485859 | G | A | 290 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(287): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.550+1866C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485859 | |||||||
| chr17:58485955 | G | A | 2 | a0003c0003t0001g0015 a0003c0003t0008g0316 |
3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.550+1770C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485955 | |||||||
| chr17:58486089 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.550+1636G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486089 | |||||||
| chr17:58486130 | A | C | 1 | a0009c0008t0001g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.550+1595T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486130 | |||||||
| chr17:58486191 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.550+1534A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486191 | |||||||
| chr17:58486314 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.550+1411C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486314 | |||||||
| chr17:58486322 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG01243.hp2 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1403C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486322 | |||||||
| chr17:58486327 | T | A | 1 | a0001c0001t0001g0293 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.550+1398A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486327 | |||||||
| chr17:58486412 | G | T | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.550+1313C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486412 | |||||||
| chr17:58486725 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0061 |
4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+1000A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486725 | |||||||
| chr17:58486887 | T | C | 1 | a0002c0002t0001g0294 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.550+838A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486887 | |||||||
| chr17:58486902 | CT | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.550+822delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486902 | |||||||
| chr17:58486902 | CTT | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0295 a0001c0001t0001g0296 others(16): Show |
20 | HG00323.hp2 HG00558.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.550+821_550+822del others(2): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486902 | |||||||
| chr17:58487196 | A | G | 2 | a0001c0001t0005g0002 a0001c0001t0010g0017 |
3 | HG02257.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+529T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487196 | |||||||
| chr17:58487303 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+422A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487303 | |||||||
| chr17:58487305 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+420A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487305 | |||||||
| chr17:58487306 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+419C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487306 | |||||||
| chr17:58487310 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+415G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487310 | |||||||
| chr17:58487313 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+412G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487313 | |||||||
| chr17:58487319 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+406G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487319 | |||||||
| chr17:58487324 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+401C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487324 | |||||||
| chr17:58487326 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+399A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487326 | |||||||
| chr17:58487327 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+398A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487327 | |||||||
| chr17:58487331 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+394G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487331 | |||||||
| chr17:58487332 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+393C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487332 | |||||||
| chr17:58487338 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+387G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487338 | |||||||
| chr17:58487339 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+386A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487339 | |||||||
| chr17:58487341 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+384G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487341 | |||||||
| chr17:58487343 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+382C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487343 | |||||||
| chr17:58487345 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+380C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487345 | |||||||
| chr17:58487347 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+378G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487347 | |||||||
| chr17:58487348 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+377G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487348 | |||||||
| chr17:58487351 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+374T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487351 | |||||||
| chr17:58487353 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+372C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487353 | |||||||
| chr17:58487355 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+370A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487355 | |||||||
| chr17:58487356 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+369A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487356 | |||||||
| chr17:58487360 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+365C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487360 | |||||||
| chr17:58487362 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+363C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487362 | |||||||
| chr17:58487364 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+361T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487364 | |||||||
| chr17:58487365 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+360G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487365 | |||||||
| chr17:58487367 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+358C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487367 | |||||||
| chr17:58487369 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+356C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487369 | |||||||
| chr17:58487374 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+351A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487374 | |||||||
| chr17:58487375 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+350G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487375 | |||||||
| chr17:58487378 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+347T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487378 | |||||||
| chr17:58487379 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+346C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487379 | |||||||
| chr17:58487380 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+345C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487380 | |||||||
| chr17:58487383 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+342C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487383 | |||||||
| chr17:58487384 | G | GAATTATC others(8): Show |
1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+340_550+341ins others(15): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487384 | |||||||
| chr17:58487387 | A | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+338T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487387 | |||||||
| chr17:58487389 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+336G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487389 | |||||||
| chr17:58487391 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+334C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487391 | |||||||
| chr17:58487397 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+328A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487397 | |||||||
| chr17:58487399 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+326G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487399 | |||||||
| chr17:58487402 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+323G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487402 | |||||||
| chr17:58487403 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+322G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487403 | |||||||
| chr17:58487405 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+320C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487405 | |||||||
| chr17:58487406 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+319C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487406 | |||||||
| chr17:58487417 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+308C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487417 | |||||||
| chr17:58487418 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+307C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487418 | |||||||
| chr17:58487419 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+306C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487419 | |||||||
| chr17:58487422 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+303G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487422 | |||||||
| chr17:58487429 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+296C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487429 | |||||||
| chr17:58487430 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+295C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487430 | |||||||
| chr17:58487433 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+292G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487433 | |||||||
| chr17:58487434 | G | A | 2 | a0001c0001t0001g0314 a0001c0004t0001g0313 |
2 | HG01346.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.550+291C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487434 | |||||||
| chr17:58487611 | C | A | 1 | a0002c0002t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.550+114G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487611 |