Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3298 |
| ensemblid | ENSG00000025156.13 |
| hgncid | 5225 |
| symbol | HSF2 |
| name | heat shock transcription factor 2 |
| refseq_nuc | NM_004506.4 |
| refseq_prot | NP_004497.1 |
| ensembl_nuc | ENST00000368455.9 |
| ensembl_prot | ENSP00000357440.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 122399652 |
| end | 122433119 |
| strand | + |
| ver | v1.2 |
| region | chr6:122399652-122433119 |
| region5000 | chr6:122394652-122438119 |
| regionname0 | HSF2_chr6_122399652_122433119 |
| regionname5000 | HSF2_chr6_122394652_122438119 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1608 | 366 | 86 | 68 | 167 | 13 | 30 | HSF2_chr6_122394652_122438119 | HSF2 | ATGAA others(1603): Show |
chr6 | 122394652 | 122438119 | ||
| a0001c0002 | 0/0 | 1608 | 13 | 0 | 0 | 13 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | ATGAA others(1603): Show |
chr6 | 122394652 | 122438119 | ||
| a0001c0003 | 0/0 | 1608 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | ATGAA others(1603): Show |
chr6 | 122394652 | 122438119 | ||
| a0001c0004 | 0/0 | 1608 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | ATGAA others(1603): Show |
chr6 | 122394652 | 122438119 | ||
| a0001c0005 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | ATGAA others(1603): Show |
chr6 | 122394652 | 122438119 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2596 | 180 | 37 | 40 | 79 | 5 | 19 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0002 | 1/0 | 2596 | 122 | 30 | 19 | 61 | 4 | 7 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0003 | 0/1 | 2608 | 53 | 11 | 8 | 26 | 3 | 4 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2603): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0004 | 0/0 | 2596 | 5 | 5 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0005 | 0/0 | 2596 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0006 | 0/0 | 2596 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0007 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0001t0008 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0002t0002 | 0/0 | 2596 | 13 | 0 | 0 | 13 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0003t0002 | 0/0 | 2596 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| a0001c0004t0003 | 0/0 | 2608 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2603): Show |
chr6 | 122394652 | 122438119 |
| a0001c0005t0001 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | GTTCT others(2591): Show |
chr6 | 122394652 | 122438119 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 0 | 18 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 8 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0008 | 0/0 | 7 | 2 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0009 | 0/0 | 7 | 1 | 4 | 0 | 1 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0003 | 0/0 | 16 | 0 | 2 | 12 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0004 | 0/0 | 12 | 2 | 1 | 9 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0027 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0002 | 0/0 | 17 | 0 | 2 | 11 | 2 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0001t0008g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0004t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0199 | EUR | GBR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0168 | EUR | GBR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01168 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01169 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0107 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18990 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0201 | REF | REF | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0027 | REF | REF | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:122412393 | C | T | 1 | a0001c0004 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.114C>T | p.Val38Val | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 2/13 | 200/2596 | 114/1611 | 38/536 | chr6 | 122412393 | |||
| chr6:122422874 | A | T | 2 | a0001c0002 a0001c0003 |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
synonymous_variant | LOW | c.987A>T | p.Leu329Leu | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/13 | 1073/2596 | 987/1611 | 329/536 | chr6 | 122422874 | |||
| chr6:122423632 | C | T | 1 | a0001c0005 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1122C>T | p.Phe374Phe | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/13 | 1208/2596 | 1122/1611 | 374/536 | chr6 | 122423632 | |||
| chr6:122431468 | A | C | 1 | a0001c0003 | 4 | HG00544.hp1 NA18612.hp2 NA18964.hp1 others(1): Show |
synonymous_variant | LOW | c.1269A>C | p.Val423Val | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/13 | 1355/2596 | 1269/1611 | 423/536 | chr6 | 122431468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:122399661 | G | A | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(2): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | 77 | chr6 | 122399661 | ||||||
| chr6:122399668 | T | TGCCGTAG others(5): Show |
2 | a0001c0001t0003 a0001c0004t0003 |
54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-65_-54dupTAGCTGCC others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | 53 | INFO_REALIGN_3_PRIME | chr6 | 122399668 | |||||
| chr6:122399671 | C | T | 1 | a0001c0001t0008 | 1 | NA19010.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399671 | |||||||
| chr6:122399704 | G | T | 1 | a0001c0001t0007 | 1 | HG01515.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399704 | |||||||
| chr6:122399728 | C | T | 1 | a0001c0001t0006 | 1 | HG01975.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399728 | |||||||
| chr6:122432223 | C | T | 1 | a0001c0001t0005 | 3 | HG02109.hp1 HG02559.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 13/13 | 3 | chr6 | 122432223 | ||||||
| chr6:122432515 | C | T | 1 | a0001c0001t0004 | 5 | HG02818.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*295C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 13/13 | 295 | chr6 | 122432515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:122399875 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93+45C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122399875 | |||||||
| chr6:122399922 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.93+92C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122399922 | |||||||
| chr6:122400064 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.93+234C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400064 | |||||||
| chr6:122400167 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93+337T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400167 | |||||||
| chr6:122400276 | G | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+446G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400276 | |||||||
| chr6:122400305 | A | G | 45 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(42): Show |
74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.93+475A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400305 | |||||||
| chr6:122400365 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.93+535A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400365 | |||||||
| chr6:122400687 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
5 | HG01081.hp1 HG01109.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+857A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400687 | |||||||
| chr6:122400747 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.93+917C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400747 | |||||||
| chr6:122400829 | G | A | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+999G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400829 | |||||||
| chr6:122401163 | G | C | 45 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(42): Show |
74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.93+1333G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401163 | |||||||
| chr6:122401374 | C | G | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+1544C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401374 | |||||||
| chr6:122401456 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1626T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401456 | |||||||
| chr6:122401585 | A | AT | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.93+1756dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122401585 | ||||||
| chr6:122401663 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0176 others(4): Show |
12 | HG01255.hp1 HG02004.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+1833A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401663 | |||||||
| chr6:122401683 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG02615.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.93+1853G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401683 | |||||||
| chr6:122401772 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.93+1942A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401772 | |||||||
| chr6:122402151 | C | A | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93+2321C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402151 | |||||||
| chr6:122402314 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+2484T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402314 | |||||||
| chr6:122402562 | G | GT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
8 | HG00609.hp1 HG01884.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+2744dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122402562 | ||||||
| chr6:122402677 | C | A | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+2847C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402677 | |||||||
| chr6:122402677 | C | G | 1 | a0001c0001t0001g0037 | 2 | NA18990.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.93+2847C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402677 | |||||||
| chr6:122402715 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93+2885G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402715 | |||||||
| chr6:122402844 | C | T | 3 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0209 |
3 | HG02083.hp2 NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.93+3014C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402844 | |||||||
| chr6:122403329 | G | A | 2 | a0001c0001t0003g0183 a0001c0001t0003g0184 |
2 | HG02080.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.93+3499G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403329 | |||||||
| chr6:122403379 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.93+3549G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403379 | |||||||
| chr6:122403454 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.93+3624G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403454 | |||||||
| chr6:122403518 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.93+3688G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403518 | |||||||
| chr6:122403754 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.93+3924G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403754 | |||||||
| chr6:122403868 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.93+4038T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403868 | |||||||
| chr6:122403918 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.93+4088T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403918 | |||||||
| chr6:122403959 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.93+4129A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403959 | |||||||
| chr6:122404264 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.93+4434C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404264 | |||||||
| chr6:122404591 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.93+4761T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404591 | |||||||
| chr6:122404598 | A | AGG | 45 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(42): Show |
74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.93+4768_93+4769ins others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404598 | |||||||
| chr6:122404726 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.93+4896C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404726 | |||||||
| chr6:122404782 | G | A | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+4952G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404782 | |||||||
| chr6:122404863 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.93+5033A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404863 | |||||||
| chr6:122405162 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.93+5332G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405162 | |||||||
| chr6:122405250 | G | A | 6 | a0001c0001t0002g0018 a0001c0001t0002g0076 a0001c0001t0002g0077 others(3): Show |
8 | NA18956.hp2 NA18960.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+5420G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405250 | |||||||
| chr6:122405252 | C | G | 1 | a0001c0001t0002g0028 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.93+5422C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405252 | |||||||
| chr6:122405256 | T | TA | 9 | a0001c0001t0001g0030 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
10 | HG01433.hp1 HG01515.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+5445dupA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122405256 | ||||||
| chr6:122405256 | TA | T | 18 | a0001c0001t0001g0044 a0001c0001t0001g0162 a0001c0001t0001g0163 others(15): Show |
19 | HG00099.hp2 HG01257.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+5445delA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122405256 | ||||||
| chr6:122405369 | A | G | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+5539A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405369 | |||||||
| chr6:122405408 | G | C | 1 | a0001c0002t0002g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.93+5578G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405408 | |||||||
| chr6:122405443 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+5613A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405443 | |||||||
| chr6:122405894 | T | C | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+6064T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405894 | |||||||
| chr6:122406310 | A | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-6063A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406310 | |||||||
| chr6:122406521 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.94-5852G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406521 | |||||||
| chr6:122406602 | G | A | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-5771G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406602 | |||||||
| chr6:122406682 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.94-5691G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406682 | |||||||
| chr6:122406775 | AG | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.94-5597delG | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406775 | |||||||
| chr6:122406819 | G | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-5554G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406819 | |||||||
| chr6:122406959 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0162 |
3 | HG00597.hp2 HG02132.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-5414G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406959 | |||||||
| chr6:122406996 | A | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.94-5377A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406996 | |||||||
| chr6:122407049 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-5324A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407049 | |||||||
| chr6:122407125 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-5248G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407125 | |||||||
| chr6:122407426 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.94-4947A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407426 | |||||||
| chr6:122407591 | GT | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.94-4771delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407591 | ||||||
| chr6:122407602 | T | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-4771T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407602 | |||||||
| chr6:122407719 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0160 |
3 | HG02027.hp1 NA18948.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.94-4654C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407719 | |||||||
| chr6:122407727 | A | G | 33 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(30): Show |
53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-4646A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407727 | |||||||
| chr6:122407734 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.94-4639A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407734 | |||||||
| chr6:122407765 | C | T | 26 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(23): Show |
46 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.94-4608C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407765 | |||||||
| chr6:122407838 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.94-4535G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407838 | |||||||
| chr6:122407885 | G | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.94-4488G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407885 | |||||||
| chr6:122407961 | C | CAG | 35 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(32): Show |
65 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.94-4387_94-4386dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | ||||||
| chr6:122407961 | C | CAGAG | 3 | a0001c0001t0002g0024 a0001c0001t0002g0052 a0001c0001t0002g0096 |
4 | HG02486.hp2 HG04199.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-4389_94-4386dup others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | ||||||
| chr6:122407961 | CAG | C | 2 | a0001c0001t0001g0160 a0001c0001t0002g0025 |
3 | HG01257.hp1 HG01258.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.94-4387_94-4386del others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | ||||||
| chr6:122407961 | CAGAG | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.94-4389_94-4386del others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | ||||||
| chr6:122408021 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.94-4352C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408021 | |||||||
| chr6:122408083 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.94-4290T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408083 | |||||||
| chr6:122408087 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.94-4286A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408087 | |||||||
| chr6:122408105 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.94-4268T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408105 | |||||||
| chr6:122408192 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-4181C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408192 | |||||||
| chr6:122408335 | T | TA | 31 | a0001c0001t0001g0060 a0001c0001t0001g0102 a0001c0001t0002g0003 others(28): Show |
55 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.94-4025dupA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122408335 | ||||||
| chr6:122408386 | A | T | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3987A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408386 | |||||||
| chr6:122408482 | G | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02027.hp2 NA19002.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.94-3891G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408482 | |||||||
| chr6:122408503 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-3870T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408503 | |||||||
| chr6:122408522 | A | C | 5 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 others(2): Show |
5 | NA18956.hp2 NA18960.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3851A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408522 | |||||||
| chr6:122408616 | A | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3757A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408616 | |||||||
| chr6:122408625 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-3748C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408625 | |||||||
| chr6:122408747 | A | G | 6 | a0001c0001t0002g0052 a0001c0001t0002g0064 a0001c0001t0002g0065 others(3): Show |
6 | HG01261.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3626A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408747 | |||||||
| chr6:122408768 | C | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3605C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408768 | |||||||
| chr6:122408848 | A | AT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
95 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.94-3509dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122408848 | ||||||
| chr6:122408877 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.94-3496T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408877 | |||||||
| chr6:122409206 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.94-3167A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409206 | |||||||
| chr6:122409280 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.94-3093G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409280 | |||||||
| chr6:122409497 | T | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.94-2876T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409497 | |||||||
| chr6:122409544 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.94-2829A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409544 | |||||||
| chr6:122409545 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.94-2828C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409545 | |||||||
| chr6:122409657 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.94-2716A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409657 | |||||||
| chr6:122409759 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0003g0218 |
8 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-2614A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409759 | |||||||
| chr6:122409813 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0108 others(4): Show |
14 | HG00323.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-2560T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409813 | |||||||
| chr6:122409873 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-2500C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409873 | |||||||
| chr6:122410261 | T | A | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.94-2112T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410261 | |||||||
| chr6:122410498 | C | T | 2 | a0001c0001t0003g0203 a0001c0001t0003g0204 |
2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.94-1875C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410498 | |||||||
| chr6:122410550 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-1823C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410550 | |||||||
| chr6:122410673 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
190 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.94-1700C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410673 | |||||||
| chr6:122410815 | T | G | 2 | a0001c0001t0003g0192 a0001c0001t0003g0193 |
2 | NA18953.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.94-1558T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410815 | |||||||
| chr6:122410945 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94-1428T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410945 | |||||||
| chr6:122410948 | G | GT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.94-1409dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | ||||||
| chr6:122410948 | G | GTT | 9 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG00621.hp2 HG00741.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-1410_94-1409dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | ||||||
| chr6:122410948 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18942.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.94-1425G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410948 | |||||||
| chr6:122410948 | GT | G | 36 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(33): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.94-1409delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | ||||||
| chr6:122411011 | T | G | 1 | a0001c0001t0003g0194 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.94-1362T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411011 | |||||||
| chr6:122411041 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0007g0107 |
2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.94-1332C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411041 | |||||||
| chr6:122411095 | T | A | 30 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(27): Show |
54 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.94-1278T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411095 | |||||||
| chr6:122411239 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.94-1134A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411239 | |||||||
| chr6:122411307 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94-1066G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411307 | |||||||
| chr6:122411323 | G | C | 1 | a0001c0001t0003g0195 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.94-1050G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411323 | |||||||
| chr6:122411327 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.94-1046T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411327 | |||||||
| chr6:122411347 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0116 |
3 | HG03704.hp1 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.94-1026T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411347 | |||||||
| chr6:122411612 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.94-761T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411612 | |||||||
| chr6:122411641 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94-732T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411641 | |||||||
| chr6:122411643 | T | G | 1 | a0001c0001t0002g0076 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.94-730T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411643 | |||||||
| chr6:122411914 | A | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-459A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411914 | |||||||
| chr6:122412025 | A | C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94-348A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412025 | |||||||
| chr6:122412127 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94-246T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412127 | |||||||
| chr6:122412362 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.94-11T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412362 | |||||||
| chr6:122412781 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+17G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412781 | |||||||
| chr6:122412822 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0117 |
3 | HG00735.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.330+58G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412822 | |||||||
| chr6:122412833 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.330+69C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412833 | |||||||
| chr6:122412909 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.330+145C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412909 | |||||||
| chr6:122412924 | A | G | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.330+160A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412924 | |||||||
| chr6:122412930 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.330+166G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412930 | |||||||
| chr6:122413090 | AT | A | 32 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(29): Show |
52 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.330+332delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 122413090 | ||||||
| chr6:122413177 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0154 |
2 | HG02165.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.331-348A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413177 | |||||||
| chr6:122413303 | C | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.331-222C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413303 | |||||||
| chr6:122413323 | A | AT | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.331-194dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 122413323 | ||||||
| chr6:122413400 | C | T | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.331-125C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413400 | |||||||
| chr6:122413775 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0137 |
3 | HG02896.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.455+126A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413775 | |||||||
| chr6:122413827 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.455+178G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413827 | |||||||
| chr6:122413975 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.455+326A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413975 | |||||||
| chr6:122413976 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.455+327T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413976 | |||||||
| chr6:122414035 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.455+386G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414035 | |||||||
| chr6:122414038 | T | G | 27 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(24): Show |
47 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.455+389T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414038 | |||||||
| chr6:122414168 | C | T | 4 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(1): Show |
4 | HG02615.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+519C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414168 | |||||||
| chr6:122414473 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0030 others(21): Show |
39 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.455+824C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414473 | |||||||
| chr6:122414545 | G | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.455+896G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414545 | |||||||
| chr6:122414800 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.455+1151A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414800 | |||||||
| chr6:122414819 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.455+1170G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414819 | |||||||
| chr6:122415097 | A | T | 1 | a0001c0001t0002g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.456-1124A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415097 | |||||||
| chr6:122415248 | A | C | 1 | a0001c0001t0003g0208 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.456-973A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415248 | |||||||
| chr6:122415281 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(30): Show |
53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.456-940T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415281 | |||||||
| chr6:122415329 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.456-892A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415329 | |||||||
| chr6:122415691 | C | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.456-530C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415691 | |||||||
| chr6:122415761 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.456-460C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415761 | |||||||
| chr6:122415779 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.456-442C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415779 | |||||||
| chr6:122415865 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.456-356A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415865 | |||||||
| chr6:122415959 | A | G | 32 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(29): Show |
52 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.456-262A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415959 | |||||||
| chr6:122416022 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.456-199T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416022 | |||||||
| chr6:122416058 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.456-163T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416058 | |||||||
| chr6:122416110 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.456-111T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416110 | |||||||
| chr6:122416171 | T | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-50T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416171 | |||||||
| chr6:122416181 | AT | A | 12 | a0001c0001t0003g0196 a0001c0001t0003g0199 a0001c0001t0003g0200 others(9): Show |
20 | HG00099.hp1 HG00544.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.456-30delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 122416181 | ||||||
| chr6:122416314 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.531+18C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416314 | |||||||
| chr6:122416490 | A | G | 1 | a0001c0001t0001g0020 | 3 | NA18974.hp1 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.531+194A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416490 | |||||||
| chr6:122416514 | G | T | 26 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(23): Show |
46 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.531+218G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416514 | |||||||
| chr6:122416604 | A | G | 5 | a0001c0001t0002g0014 a0001c0001t0002g0081 a0001c0001t0004g0014 others(2): Show |
7 | HG02451.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+308A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416604 | |||||||
| chr6:122416786 | G | C | 1 | a0001c0001t0003g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.531+490G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416786 | |||||||
| chr6:122417124 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(30): Show |
53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.531+828G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417124 | |||||||
| chr6:122417770 | A | G | 4 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(1): Show |
4 | HG02615.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-1398A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417770 | |||||||
| chr6:122417914 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.532-1254G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417914 | |||||||
| chr6:122417917 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.532-1251T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417917 | |||||||
| chr6:122417930 | T | G | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.532-1238T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417930 | |||||||
| chr6:122417964 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.532-1204A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417964 | |||||||
| chr6:122417999 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.532-1169T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417999 | |||||||
| chr6:122418005 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.532-1163A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418005 | |||||||
| chr6:122418019 | T | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-1149T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418019 | |||||||
| chr6:122418032 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.532-1136T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418032 | |||||||
| chr6:122418142 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.532-1026G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418142 | |||||||
| chr6:122418178 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.532-990C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418178 | |||||||
| chr6:122418198 | C | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.532-970C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418198 | |||||||
| chr6:122418400 | A | G | 1 | a0001c0002t0002g0042 | 2 | NA18940.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.532-768A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418400 | |||||||
| chr6:122418477 | G | A | 10 | a0001c0001t0003g0217 a0001c0002t0002g0010 a0001c0002t0002g0023 others(7): Show |
18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.532-691G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418477 | |||||||
| chr6:122418533 | A | C | 1 | a0001c0001t0004g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.532-635A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418533 | |||||||
| chr6:122418670 | C | T | 32 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(29): Show |
52 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.532-498C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418670 | |||||||
| chr6:122418699 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.532-469T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418699 | |||||||
| chr6:122418711 | A | G | 4 | a0001c0001t0003g0198 a0001c0001t0003g0202 a0001c0001t0003g0203 others(1): Show |
4 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-457A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418711 | |||||||
| chr6:122418790 | C | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.532-378C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418790 | |||||||
| chr6:122419280 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.593+51T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419280 | |||||||
| chr6:122419295 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.593+66T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419295 | |||||||
| chr6:122419329 | G | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.593+100G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419329 | |||||||
| chr6:122419387 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.593+158T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419387 | |||||||
| chr6:122419447 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.593+218C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419447 | |||||||
| chr6:122419501 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.593+272A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419501 | |||||||
| chr6:122419557 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.593+328T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419557 | |||||||
| chr6:122419645 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.593+416T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419645 | |||||||
| chr6:122420227 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18986.hp1 | splice_region_variant&intron_variant | LOW | c.681+5T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420227 | |||||||
| chr6:122420233 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.681+11A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420233 | |||||||
| chr6:122420368 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.681+146A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420368 | |||||||
| chr6:122420637 | C | CTT | 34 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(31): Show |
56 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+422_681+423dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420637 | ||||||
| chr6:122420637 | C | CTTT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.681+421_681+423dup others(3): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420637 | ||||||
| chr6:122420700 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.681+507dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | C | CTT | 23 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0060 others(20): Show |
25 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681+506_681+507dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | C | CTTT | 10 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0150 others(7): Show |
12 | HG00099.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+505_681+507dup others(3): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | C | CTTTT | 18 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0183 others(15): Show |
35 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.681+504_681+507dup others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | C | CTTTTT | 7 | a0001c0001t0003g0041 a0001c0001t0003g0190 a0001c0001t0003g0191 others(4): Show |
8 | HG00423.hp2 HG00642.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+503_681+507dup others(5): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | CTTTTTTT | C | 9 | a0001c0001t0003g0217 a0001c0002t0002g0010 a0001c0002t0002g0023 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+501_681+507del others(7): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420700 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681+498_681+507del others(10): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | ||||||
| chr6:122420713 | T | C | 8 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(5): Show |
16 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+491T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420713 | |||||||
| chr6:122420714 | T | C | 1 | a0001c0002t0002g0213 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.681+492T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420714 | |||||||
| chr6:122420738 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.681+516A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420738 | |||||||
| chr6:122420796 | C | T | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+574C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420796 | |||||||
| chr6:122420888 | A | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.681+666A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420888 | |||||||
| chr6:122421048 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.681+826G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421048 | |||||||
| chr6:122421230 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.682-920A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421230 | |||||||
| chr6:122421239 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.682-911C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421239 | |||||||
| chr6:122421439 | G | GTAAGTGG others(18): Show |
18 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): Show |
24 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.682-709_682-685dup others(25): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122421439 | ||||||
| chr6:122421808 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.682-342G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421808 | |||||||
| chr6:122421820 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-330G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421820 | |||||||
| chr6:122422046 | C | T | 5 | a0001c0001t0002g0014 a0001c0001t0002g0081 a0001c0001t0004g0014 others(2): Show |
7 | HG02451.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-104C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122422046 | |||||||
| chr6:122422048 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.682-102A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122422048 | |||||||
| chr6:122422357 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.830+59T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422357 | |||||||
| chr6:122422368 | AC | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0160 |
5 | HG02027.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.830+71delC | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422368 | |||||||
| chr6:122422541 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0030 others(27): Show |
45 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.831-177A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422541 | |||||||
| chr6:122422542 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831-176A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422542 | |||||||
| chr6:122422548 | A | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.831-170A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422548 | |||||||
| chr6:122422558 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.831-160A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422558 | |||||||
| chr6:122422593 | C | T | 10 | a0001c0001t0003g0217 a0001c0002t0002g0010 a0001c0002t0002g0023 others(7): Show |
18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.831-125C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422593 | |||||||
| chr6:122422659 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831-59T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422659 | |||||||
| chr6:122423018 | C | G | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1070+61C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423018 | |||||||
| chr6:122423023 | T | C | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.1070+66T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423023 | |||||||
| chr6:122423043 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1070+86T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423043 | |||||||
| chr6:122423062 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0124 a0001c0001t0001g0128 others(5): Show |
16 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1070+105T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423062 | |||||||
| chr6:122423278 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0003g0218 |
8 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071-303C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423278 | |||||||
| chr6:122423295 | G | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071-286G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423295 | |||||||
| chr6:122423357 | G | A | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1071-224G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423357 | |||||||
| chr6:122423565 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071-16A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423565 | |||||||
| chr6:122423566 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071-15T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423566 | |||||||
| chr6:122423864 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1176+178A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423864 | |||||||
| chr6:122423898 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1176+212T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423898 | |||||||
| chr6:122423970 | C | G | 1 | a0001c0001t0002g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1176+284C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423970 | |||||||
| chr6:122424284 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+598A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424284 | |||||||
| chr6:122424457 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1176+771T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424457 | |||||||
| chr6:122424505 | A | G | 10 | a0001c0001t0003g0217 a0001c0002t0002g0010 a0001c0002t0002g0023 others(7): Show |
18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1176+819A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424505 | |||||||
| chr6:122424667 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1176+981A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424667 | |||||||
| chr6:122424843 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1176+1157C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424843 | |||||||
| chr6:122424989 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1176+1303T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424989 | |||||||
| chr6:122425259 | A | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+1573A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425259 | |||||||
| chr6:122425313 | G | A | 17 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0018 others(14): Show |
37 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1176+1627G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425313 | |||||||
| chr6:122425333 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1176+1647C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425333 | |||||||
| chr6:122425438 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1176+1752T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425438 | |||||||
| chr6:122425621 | G | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1176+1935G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425621 | |||||||
| chr6:122425751 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1176+2065G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425751 | |||||||
| chr6:122425768 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1176+2082A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425768 | |||||||
| chr6:122425793 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1176+2107G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425793 | |||||||
| chr6:122425860 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1177-2043A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425860 | |||||||
| chr6:122426006 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-1897G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426006 | |||||||
| chr6:122426237 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0220 |
2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1177-1666T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426237 | |||||||
| chr6:122426371 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0005g0016 |
5 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177-1532C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426371 | |||||||
| chr6:122426383 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1177-1520T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426383 | |||||||
| chr6:122426469 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1177-1434C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426469 | |||||||
| chr6:122426565 | C | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0061 a0001c0001t0002g0072 others(1): Show |
11 | HG02080.hp1 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1177-1338C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426565 | |||||||
| chr6:122426823 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1177-1080C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426823 | |||||||
| chr6:122426969 | G | A | 29 | a0001c0001t0001g0060 a0001c0001t0002g0003 a0001c0001t0002g0007 others(26): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1177-934G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426969 | |||||||
| chr6:122427096 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1177-807C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427096 | |||||||
| chr6:122427125 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1177-778T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427125 | |||||||
| chr6:122427147 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1177-756A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427147 | |||||||
| chr6:122427486 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-417G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427486 | |||||||
| chr6:122427666 | C | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0023 a0001c0002t0002g0042 others(6): Show |
17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.1177-237C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427666 | |||||||
| chr6:122427718 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1177-185G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427718 | |||||||
| chr6:122428011 | G | GTC | 34 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(31): Show |
55 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1230+56_1230+57dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122428011 | ||||||
| chr6:122428098 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1230+142T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428098 | |||||||
| chr6:122428228 | G | T | 1 | a0001c0001t0002g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1230+272G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428228 | |||||||
| chr6:122428412 | A | G | 32 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(29): Show |
52 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1230+456A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428412 | |||||||
| chr6:122428505 | G | A | 1 | a0001c0003t0002g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1230+549G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428505 | |||||||
| chr6:122428748 | A | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1230+792A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428748 | |||||||
| chr6:122428931 | A | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+975A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428931 | |||||||
| chr6:122429122 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1230+1166A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429122 | |||||||
| chr6:122429273 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0026 |
8 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1230+1317C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429273 | |||||||
| chr6:122429828 | T | G | 1 | a0001c0003t0002g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1231-1602T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429828 | |||||||
| chr6:122429859 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-1571G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429859 | |||||||
| chr6:122430224 | A | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1231-1206A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430224 | |||||||
| chr6:122430316 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1231-1114G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430316 | |||||||
| chr6:122430664 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1231-766G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430664 | |||||||
| chr6:122430793 | G | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1231-637G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430793 | |||||||
| chr6:122431042 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1231-388T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431042 | |||||||
| chr6:122431302 | C | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0003g0002 others(41): Show |
73 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1231-128C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431302 | |||||||
| chr6:122431326 | A | G | 33 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0022 others(30): Show |
53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1231-104A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431326 | |||||||
| chr6:122431405 | T | TTA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1231-15_1231-14dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122431405 | ||||||
| chr6:122431415 | A | ATT | 6 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0146 others(3): Show |
6 | HG02027.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1231-9_1231-8dupTT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122431415 | ||||||
| chr6:122431424 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG00423.hp1 | splice_region_variant&intron_variant | LOW | c.1231-6T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431424 | |||||||
| chr6:122431559 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0166 |
2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1315+45C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | chr6 | 122431559 | |||||||
| chr6:122431684 | G | GT | 104 | a0001c0001t0001g0060 a0001c0001t0001g0125 a0001c0001t0001g0140 others(101): Show |
176 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1315+182dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 122431684 | ||||||
| chr6:122431684 | G | GTT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1315+181_1315+182d others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 122431684 | ||||||
| chr6:122431789 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1316-136G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | chr6 | 122431789 |