Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3297 |
| ensemblid | ENSG00000185122.11 |
| hgncid | 5224 |
| symbol | HSF1 |
| name | heat shock transcription factor 1 |
| refseq_nuc | NM_005526.4 |
| refseq_prot | NP_005517.1 |
| ensembl_nuc | ENST00000528838.6 |
| ensembl_prot | ENSP00000431512.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 144291604 |
| end | 144314720 |
| strand | + |
| ver | v1.2 |
| region | chr8:144291604-144314720 |
| region5000 | chr8:144286604-144319720 |
| regionname0 | HSF1_chr8_144291604_144314720 |
| regionname5000 | HSF1_chr8_144286604_144319720 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 529 | 312 | 88 | 52 | 120 | 14 | 37 | 77 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0002 | 0/1 | 529 | 12 | 0 | 2 | 4 | 0 | 5 | 4 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0003 | 0/0 | 529 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0004 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0005 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0006 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| a0007 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | MDLPV others(524): Show |
chr8 | 144286604 | 144319720 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1587 | 307 | 85 | 51 | 120 | 14 | 36 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0001c0003 | 0/0 | 1587 | 3 | 2 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0001c0006 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0001c0009 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0002c0002 | 0/1 | 1587 | 12 | 0 | 2 | 4 | 0 | 5 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0003c0004 | 0/0 | 1587 | 2 | 0 | 2 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0004c0007 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0005c0005 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0006c0008 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 | ||
| a0007c0010 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | ATGGA others(1582): Show |
chr8 | 144286604 | 144319720 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2134 | 297 | 77 | 51 | 119 | 14 | 35 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0002 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0004 | 0/0 | 2134 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0005 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0006 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0007 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0008 | 0/0 | 2134 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0009 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0001t0010 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0003t0001 | 0/0 | 2134 | 3 | 2 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0006t0001 | 0/0 | 2134 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0001c0009t0001 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0002c0002t0001 | 0/1 | 2134 | 12 | 0 | 2 | 4 | 0 | 5 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0003c0004t0001 | 0/0 | 2134 | 2 | 0 | 2 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0004c0007t0001 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0005c0005t0001 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0006c0008t0003 | 0/0 | 2134 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| a0007c0010t0001 | 0/0 | 2134 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | CGTTG others(2129): Show |
chr8 | 144286604 | 144319720 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 2 | 7 | 1 | 3 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0001c0009t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0003c0004t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0004c0007t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0005c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0006c0008t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| a0007c0010t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | GBR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01069 | hp2 | a0003 | c0004 | t0001 | g0028 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01071 | hp2 | a0003 | c0004 | t0001 | g0028 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0231 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02280 | hp2 | a0001 | c0009 | t0001 | g0058 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0241 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02886 | hp2 | a0004 | c0007 | t0001 | g0129 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0200 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03704 | hp1 | a0001 | c0006 | t0001 | g0087 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0254 | SAS | BEB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18522 | hp2 | a0005 | c0005 | t0001 | g0075 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18747 | hp1 | a0006 | c0008 | t0003 | g0117 | EAS | CHB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | GIH | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | GIH | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | USA | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA18955 | hp2 | a0007 | c0010 | t0001 | g0088 | EAS | JPT | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0225 | REF | REF | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0055 | REF | REF | HSF1_chr8_144286604_144319720 | HSF1 | chr8 | 144286604 | 144319720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144291779 | G | C | 1 | a0007 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.22G>C | p.Gly8Arg | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/13 | 176/2134 | 22/1590 | 8/529 | chr8 | 144291779 | |||
| chr8:144311521 | G | A | 1 | a0003 | 2 | HG01069.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.643G>A | p.Asp215Asn | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 7/13 | 797/2134 | 643/1590 | 215/529 | chr8 | 144311521 | |||
| chr8:144311970 | T | C | 1 | a0005 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.868T>C | p.Ser290Pro | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/13 | 1022/2134 | 868/1590 | 290/529 | chr8 | 144311970 | |||
| chr8:144312181 | G | A | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1079G>A | p.Arg360Gln | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/13 | 1233/2134 | 1079/1590 | 360/529 | chr8 | 144312181 | |||
| chr8:144312195 | C | A | 2 | a0002 a0003 |
13 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(10): Show |
missense_variant | MODERATE | c.1093C>A | p.Pro365Thr | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/13 | 1247/2134 | 1093/1590 | 365/529 | chr8 | 144312195 | |||
| chr8:144314046 | C | T | 1 | a0006 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1376C>T | p.Pro459Leu | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 12/13 | 1530/2134 | 1376/1590 | 459/529 | chr8 | 144314046 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144291778 | C | G | 1 | a0007c0010 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.21C>G | p.Pro7Pro | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/13 | 175/2134 | 21/1590 | 7/529 | chr8 | 144291778 | |||
| chr8:144291829 | C | A | 1 | a0001c0003 | 3 | HG01175.hp1 HG02451.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.72C>A | p.Thr24Thr | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/13 | 226/2134 | 72/1590 | 24/529 | chr8 | 144291829 | |||
| chr8:144311813 | C | T | 1 | a0001c0009 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.837C>T | p.Ser279Ser | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 8/13 | 991/2134 | 837/1590 | 279/529 | chr8 | 144311813 | |||
| chr8:144312041 | G | A | 1 | a0001c0006 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.939G>A | p.Ala313Ala | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/13 | 1093/2134 | 939/1590 | 313/529 | chr8 | 144312041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144291634 | C | T | 1 | a0001c0001t0010 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/13 | 124 | chr8 | 144291634 | ||||||
| chr8:144314355 | C | T | 1 | a0001c0001t0009 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 25 | chr8 | 144314355 | ||||||
| chr8:144314439 | T | C | 1 | a0006c0008t0003 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 109 | chr8 | 144314439 | ||||||
| chr8:144314450 | G | A | 1 | a0001c0001t0002 | 3 | HG02647.hp2 HG02809.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*120G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 120 | chr8 | 144314450 | ||||||
| chr8:144314481 | C | G | 1 | a0001c0001t0009 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*151C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 151 | chr8 | 144314481 | ||||||
| chr8:144314616 | T | A | 1 | a0001c0001t0004 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 286 | chr8 | 144314616 | ||||||
| chr8:144314636 | C | T | 1 | a0001c0001t0008 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 306 | chr8 | 144314636 | ||||||
| chr8:144314641 | C | G | 1 | a0001c0001t0007 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 311 | chr8 | 144314641 | ||||||
| chr8:144314678 | C | T | 1 | a0001c0001t0006 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 348 | chr8 | 144314678 | ||||||
| chr8:144314714 | T | G | 1 | a0001c0001t0005 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 13/13 | 384 | chr8 | 144314714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144291909 | A | T | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+35A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144291909 | |||||||
| chr8:144291932 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.117+58C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144291932 | |||||||
| chr8:144292105 | C | G | 1 | a0001c0003t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.117+231C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292105 | |||||||
| chr8:144292305 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.117+431G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292305 | |||||||
| chr8:144292381 | G | T | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+507G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292381 | |||||||
| chr8:144292487 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.117+613C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292487 | |||||||
| chr8:144292545 | A | G | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG02074.hp1 NA18955.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+671A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292545 | |||||||
| chr8:144292566 | T | A | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+692T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292566 | |||||||
| chr8:144292748 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.117+874G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292748 | |||||||
| chr8:144292778 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.117+904T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292778 | |||||||
| chr8:144292808 | A | T | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+934A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292808 | |||||||
| chr8:144292911 | A | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.117+1037A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292911 | |||||||
| chr8:144292953 | TAAGAAAA others(2): Show |
T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.117+1095_117+1103d others(11): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144292953 | ||||||
| chr8:144292965 | GAAAAAAA others(3): Show |
G | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+1094_117+1103d others(12): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144292965 | ||||||
| chr8:144292995 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.117+1121A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144292995 | |||||||
| chr8:144293016 | C | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.117+1142C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293016 | |||||||
| chr8:144293104 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+1230G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293104 | |||||||
| chr8:144293266 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.117+1392T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293266 | |||||||
| chr8:144293437 | T | TC | 2 | a0001c0001t0001g0005 a0001c0001t0001g0147 |
5 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1564dupC | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144293437 | ||||||
| chr8:144293439 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+1565T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293439 | |||||||
| chr8:144293444 | TC | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+1571delC | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293444 | |||||||
| chr8:144293445 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+1571C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293445 | |||||||
| chr8:144293446 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+1572T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293446 | |||||||
| chr8:144293554 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.117+1680C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293554 | |||||||
| chr8:144293795 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117+1921T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293795 | |||||||
| chr8:144293813 | C | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.117+1939C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293813 | |||||||
| chr8:144293813 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.117+1939C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144293813 | |||||||
| chr8:144294201 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.117+2327G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294201 | |||||||
| chr8:144294231 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02738.hp1 HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.117+2357C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294231 | |||||||
| chr8:144294600 | G | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0035 others(6): Show |
10 | HG01192.hp2 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+2726G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294600 | |||||||
| chr8:144294733 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.117+2859A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294733 | |||||||
| chr8:144294763 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.117+2889C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294763 | |||||||
| chr8:144294769 | CT | C | 2 | a0001c0001t0001g0011 a0002c0002t0001g0271 |
3 | HG01256.hp1 HG01258.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.117+2896delT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294769 | |||||||
| chr8:144294895 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+3021G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144294895 | |||||||
| chr8:144295077 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.117+3203C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295077 | |||||||
| chr8:144295095 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0150 |
3 | HG03491.hp2 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.117+3221T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295095 | |||||||
| chr8:144295160 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.117+3286A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295160 | |||||||
| chr8:144295301 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG00733.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.117+3427C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295301 | |||||||
| chr8:144295318 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+3444C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295318 | |||||||
| chr8:144295352 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.117+3478G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295352 | |||||||
| chr8:144295432 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.117+3558C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295432 | |||||||
| chr8:144295713 | C | CTT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+3852_117+3853d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144295713 | ||||||
| chr8:144295744 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+3870T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295744 | |||||||
| chr8:144295750 | CAG | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01934.hp2 NA18612.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+3877_117+3878d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295750 | |||||||
| chr8:144295789 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.117+3915C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295789 | |||||||
| chr8:144295859 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.117+3985G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295859 | |||||||
| chr8:144295955 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.117+4081C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144295955 | |||||||
| chr8:144296005 | G | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.117+4131G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296005 | |||||||
| chr8:144296046 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+4172T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296046 | |||||||
| chr8:144296171 | A | C | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+4297A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296171 | |||||||
| chr8:144296173 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.117+4299G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296173 | |||||||
| chr8:144296176 | C | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.117+4302C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296176 | |||||||
| chr8:144296281 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.117+4407T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296281 | |||||||
| chr8:144296287 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.117+4413A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296287 | |||||||
| chr8:144296322 | C | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.117+4448C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296322 | |||||||
| chr8:144296477 | T | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.117+4603T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296477 | |||||||
| chr8:144296566 | A | T | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+4692A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296566 | |||||||
| chr8:144296806 | C | CA | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00438.hp2 HG01071.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+4947dupA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144296806 | ||||||
| chr8:144296806 | CA | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.117+4947delA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144296806 | ||||||
| chr8:144296808 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.117+4934A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296808 | |||||||
| chr8:144296824 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.117+4950A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296824 | |||||||
| chr8:144296874 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+5000A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296874 | |||||||
| chr8:144296917 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.117+5043G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296917 | |||||||
| chr8:144296927 | T | TG | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.117+5061dupG | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144296927 | ||||||
| chr8:144296930 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+5056G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296930 | |||||||
| chr8:144296938 | C | T | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+5064C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144296938 | |||||||
| chr8:144297072 | G | T | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.117+5198G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297072 | |||||||
| chr8:144297147 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02132.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.117+5273C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297147 | |||||||
| chr8:144297175 | GAAGC | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+5307_117+5310d others(6): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144297175 | ||||||
| chr8:144297250 | G | A | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+5376G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297250 | |||||||
| chr8:144297349 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117+5475T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297349 | |||||||
| chr8:144297482 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+5608A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297482 | |||||||
| chr8:144297590 | G | C | 1 | a0002c0002t0001g0161 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.117+5716G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297590 | |||||||
| chr8:144297632 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.117+5758C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297632 | |||||||
| chr8:144297697 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+5823G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297697 | |||||||
| chr8:144297844 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+5970G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144297844 | |||||||
| chr8:144298028 | T | A | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+6154T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298028 | |||||||
| chr8:144298260 | T | A | 1 | a0002c0002t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.117+6386T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298260 | |||||||
| chr8:144298301 | C | T | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+6427C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298301 | |||||||
| chr8:144298440 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.117+6566T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298440 | |||||||
| chr8:144298442 | C | CA | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.117+6582dupA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144298442 | ||||||
| chr8:144298466 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+6592G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298466 | |||||||
| chr8:144298482 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.117+6608G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298482 | |||||||
| chr8:144298537 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.117+6663A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298537 | |||||||
| chr8:144298546 | A | C | 1 | a0001c0001t0008g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.117+6672A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298546 | |||||||
| chr8:144298553 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0249 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.117+6679C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298553 | |||||||
| chr8:144298569 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.117+6695C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298569 | |||||||
| chr8:144298586 | G | A | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+6712G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298586 | |||||||
| chr8:144298598 | C | CA | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+6737dupA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144298598 | ||||||
| chr8:144298608 | AAAAG | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0035 others(10): Show |
14 | HG01192.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+6742_117+6745d others(6): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144298608 | ||||||
| chr8:144298658 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.117+6784G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298658 | |||||||
| chr8:144298663 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.117+6789G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298663 | |||||||
| chr8:144298693 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.117+6819C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298693 | |||||||
| chr8:144298696 | G | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.117+6822G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298696 | |||||||
| chr8:144298747 | T | C | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+6873T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298747 | |||||||
| chr8:144298797 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0070 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.117+6923C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298797 | |||||||
| chr8:144298812 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.117+6938C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298812 | |||||||
| chr8:144298820 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6946C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298820 | |||||||
| chr8:144298871 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.117+6997G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298871 | |||||||
| chr8:144298946 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02572.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.117+7072C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144298946 | |||||||
| chr8:144299056 | C | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.117+7182C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299056 | |||||||
| chr8:144299130 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG02129.hp2 NA18747.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.117+7256G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299130 | |||||||
| chr8:144299208 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+7334G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299208 | |||||||
| chr8:144299251 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+7377G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299251 | |||||||
| chr8:144299291 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.117+7417G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299291 | |||||||
| chr8:144299301 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG01891.hp1 HG02300.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+7427G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299301 | |||||||
| chr8:144299362 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.117+7488G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299362 | |||||||
| chr8:144299385 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+7511C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299385 | |||||||
| chr8:144299391 | C | T | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+7517C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299391 | |||||||
| chr8:144299435 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.117+7578dupA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144299435 | ||||||
| chr8:144299435 | TA | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0151 a0001c0001t0001g0242 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7578delA | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144299435 | ||||||
| chr8:144299453 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+7579T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299453 | |||||||
| chr8:144299457 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.117+7583C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299457 | |||||||
| chr8:144299532 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.117+7658G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299532 | |||||||
| chr8:144299649 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+7775C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299649 | |||||||
| chr8:144299675 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.117+7801C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299675 | |||||||
| chr8:144299720 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+7846T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299720 | |||||||
| chr8:144299724 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+7850A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299724 | |||||||
| chr8:144299864 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0113 |
6 | NA18970.hp1 NA19063.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+7990G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144299864 | |||||||
| chr8:144300006 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.117+8132A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300006 | |||||||
| chr8:144300058 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.117+8184C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300058 | |||||||
| chr8:144300201 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+8327T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300201 | |||||||
| chr8:144300212 | C | CT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.117+8361dupT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144300212 | ||||||
| chr8:144300212 | C | CTT | 29 | a0001c0001t0001g0032 a0001c0001t0001g0111 a0001c0001t0001g0145 others(26): Show |
30 | HG00597.hp1 HG00735.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.117+8360_117+8361d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144300212 | ||||||
| chr8:144300407 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.118-8499T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300407 | |||||||
| chr8:144300419 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.118-8487G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300419 | |||||||
| chr8:144300424 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0071 |
3 | HG02109.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.118-8482A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300424 | |||||||
| chr8:144300483 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-8423T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300483 | |||||||
| chr8:144300490 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0071 |
5 | HG02109.hp2 HG02145.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-8416C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300490 | |||||||
| chr8:144300517 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.118-8389G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300517 | |||||||
| chr8:144300557 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.118-8349T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300557 | |||||||
| chr8:144300809 | G | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.118-8097G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300809 | |||||||
| chr8:144300936 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-7970C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144300936 | |||||||
| chr8:144301020 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.118-7886A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301020 | |||||||
| chr8:144301032 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0113 |
6 | NA18970.hp1 NA19063.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-7874G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301032 | |||||||
| chr8:144301048 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01891.hp1 HG02300.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-7858C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301048 | |||||||
| chr8:144301175 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.118-7731C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301175 | |||||||
| chr8:144301187 | C | T | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118-7719C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301187 | |||||||
| chr8:144301199 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0226 a0001c0001t0001g0248 |
4 | HG00735.hp2 HG01106.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-7707G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301199 | |||||||
| chr8:144301312 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.118-7594G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301312 | |||||||
| chr8:144301480 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.118-7426A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301480 | |||||||
| chr8:144301527 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.118-7379A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301527 | |||||||
| chr8:144301555 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.118-7351T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301555 | |||||||
| chr8:144301589 | G | A | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118-7317G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301589 | |||||||
| chr8:144301594 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.118-7312C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301594 | |||||||
| chr8:144301633 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-7273A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301633 | |||||||
| chr8:144301703 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-7203G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301703 | |||||||
| chr8:144301721 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.118-7185C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301721 | |||||||
| chr8:144301722 | G | A | 1 | a0005c0005t0001g0075 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.118-7184G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301722 | |||||||
| chr8:144301733 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.118-7173C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301733 | |||||||
| chr8:144301844 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-7062G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301844 | |||||||
| chr8:144301893 | C | T | 8 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0220 others(5): Show |
8 | HG02165.hp2 HG02698.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-7013C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301893 | |||||||
| chr8:144301894 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.118-7012G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301894 | |||||||
| chr8:144301894 | GTGCACGG others(1697): Show |
G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG02165.hp2 HG02698.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7011_118-5308d others(2): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144301894 | |||||||
| chr8:144302059 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.118-6847G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302059 | |||||||
| chr8:144302114 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-6792C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302114 | |||||||
| chr8:144302127 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0158 |
5 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-6779T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302127 | |||||||
| chr8:144302156 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.118-6750A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302156 | |||||||
| chr8:144302161 | G | A | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118-6745G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302161 | |||||||
| chr8:144302214 | A | C | 1 | a0001c0001t0005g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.118-6692A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302214 | |||||||
| chr8:144302219 | T | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.118-6687T>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302219 | |||||||
| chr8:144302238 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-6668G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302238 | |||||||
| chr8:144302358 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0085 others(2): Show |
6 | HG00597.hp2 HG00609.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-6548T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302358 | |||||||
| chr8:144302404 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0264 a0001c0001t0001g0265 others(4): Show |
8 | HG02071.hp2 HG02074.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-6502G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302404 | |||||||
| chr8:144302449 | G | A | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118-6457G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302449 | |||||||
| chr8:144302599 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118-6307G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302599 | |||||||
| chr8:144302714 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0071 |
5 | HG02109.hp2 HG02145.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-6192C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302714 | |||||||
| chr8:144302950 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.118-5956G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144302950 | |||||||
| chr8:144303154 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0035 others(6): Show |
10 | HG01192.hp2 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-5752C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144303154 | |||||||
| chr8:144303599 | C | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG02165.hp2 HG02698.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5307C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144303599 | |||||||
| chr8:144303600 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.118-5306A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144303600 | |||||||
| chr8:144303601 | G | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG02165.hp2 HG02698.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5305G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144303601 | |||||||
| chr8:144303604 | A | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG02165.hp2 HG02698.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5302A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144303604 | |||||||
| chr8:144304140 | TGAGGG | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.118-4762_118-4758d others(7): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144304140 | ||||||
| chr8:144304397 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.118-4509C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304397 | |||||||
| chr8:144304438 | C | T | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-4468C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304438 | |||||||
| chr8:144304490 | G | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0158 |
5 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4416G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304490 | |||||||
| chr8:144304603 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.118-4303G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304603 | |||||||
| chr8:144304710 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4196G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304710 | |||||||
| chr8:144304801 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
10 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-4105G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304801 | |||||||
| chr8:144304935 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.118-3971G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304935 | |||||||
| chr8:144304947 | C | CT | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.118-3944dupT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144304947 | ||||||
| chr8:144304947 | C | CTT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0146 others(1): Show |
7 | HG00438.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3945_118-3944d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144304947 | ||||||
| chr8:144304999 | G | A | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-3907G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144304999 | |||||||
| chr8:144305008 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.118-3898G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305008 | |||||||
| chr8:144305009 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.118-3897G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305009 | |||||||
| chr8:144305021 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-3885C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305021 | |||||||
| chr8:144305040 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.118-3866T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305040 | |||||||
| chr8:144305357 | T | C | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118-3549T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305357 | |||||||
| chr8:144305689 | C | T | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-3217C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305689 | |||||||
| chr8:144305723 | A | AT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0029 others(24): Show |
29 | HG01070.hp2 HG01074.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.118-3156dupT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305723 | A | ATT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.118-3157_118-3156d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305723 | A | ATTT | 15 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0066 others(12): Show |
16 | HG00438.hp2 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.118-3158_118-3156d others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305723 | AT | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.118-3156delT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305723 | ATT | A | 12 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
12 | HG01255.hp1 HG01256.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.118-3157_118-3156d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305723 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-3167_118-3156d others(14): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144305723 | ||||||
| chr8:144305763 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.118-3143C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305763 | |||||||
| chr8:144305796 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0210 |
3 | HG02258.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.118-3110G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305796 | |||||||
| chr8:144305833 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-3073A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305833 | |||||||
| chr8:144305890 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.118-3016A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305890 | |||||||
| chr8:144305932 | AT | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2973delT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305932 | |||||||
| chr8:144305996 | T | C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2910T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144305996 | |||||||
| chr8:144306028 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.118-2878G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306028 | |||||||
| chr8:144306039 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-2867T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306039 | |||||||
| chr8:144306061 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.118-2845A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306061 | |||||||
| chr8:144306087 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0158 |
5 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-2819T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306087 | |||||||
| chr8:144306089 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-2817C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306089 | |||||||
| chr8:144306090 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.118-2816G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306090 | |||||||
| chr8:144306208 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.118-2698T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306208 | |||||||
| chr8:144306220 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.118-2686C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306220 | |||||||
| chr8:144306248 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-2658G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306248 | |||||||
| chr8:144306254 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2652T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306254 | |||||||
| chr8:144306278 | C | CT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0001g0100 others(3): Show |
6 | HG00597.hp1 HG01243.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-2615dupT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144306278 | ||||||
| chr8:144306294 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-2612C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306294 | |||||||
| chr8:144306341 | A | AT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0146 a0001c0001t0001g0147 |
6 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-2554dupT | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144306341 | ||||||
| chr8:144306373 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02738.hp1 HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.118-2533T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306373 | |||||||
| chr8:144306444 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0070 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.118-2462C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306444 | |||||||
| chr8:144306553 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0005c0005t0001g0075 |
4 | HG02055.hp1 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2353G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306553 | |||||||
| chr8:144306682 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.118-2224C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306682 | |||||||
| chr8:144306826 | C | T | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118-2080C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306826 | |||||||
| chr8:144306917 | C | CTG | 8 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0115 others(5): Show |
8 | HG02080.hp2 HG02083.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-1969_118-1968d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144306917 | ||||||
| chr8:144306946 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.118-1960G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306946 | |||||||
| chr8:144306958 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.118-1948C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144306958 | |||||||
| chr8:144307156 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.118-1750G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307156 | |||||||
| chr8:144307287 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118-1619G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307287 | |||||||
| chr8:144307649 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.118-1257A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307649 | |||||||
| chr8:144307704 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.118-1202C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307704 | |||||||
| chr8:144307730 | A | C | 1 | a0002c0002t0001g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118-1176A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307730 | |||||||
| chr8:144307742 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0031 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-1164G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307742 | |||||||
| chr8:144307919 | T | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.118-987T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144307919 | |||||||
| chr8:144308151 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0076 others(6): Show |
10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-755G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308151 | |||||||
| chr8:144308215 | G | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0059 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-691G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308215 | |||||||
| chr8:144308221 | G | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0059 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-685G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308221 | |||||||
| chr8:144308413 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.118-493G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308413 | |||||||
| chr8:144308425 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-481G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308425 | |||||||
| chr8:144308482 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.118-424C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308482 | |||||||
| chr8:144308544 | GTGCTTTG others(30): Show |
G | 1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118-344_118-308del others(37): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 144308544 | ||||||
| chr8:144308721 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
7 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-185C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308721 | |||||||
| chr8:144308722 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-184G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 1/12 | chr8 | 144308722 | |||||||
| chr8:144309220 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0005c0005t0001g0075 |
4 | HG02055.hp1 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+206G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 2/12 | chr8 | 144309220 | |||||||
| chr8:144309343 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.227-112G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 2/12 | chr8 | 144309343 | |||||||
| chr8:144309364 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-91G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 2/12 | chr8 | 144309364 | |||||||
| chr8:144309368 | C | T | 1 | a0007c0010t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.227-87C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 2/12 | chr8 | 144309368 | |||||||
| chr8:144309748 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364-24C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 3/12 | chr8 | 144309748 | |||||||
| chr8:144310129 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.488+233G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310129 | |||||||
| chr8:144310189 | C | T | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+293C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310189 | |||||||
| chr8:144310288 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.488+392T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310288 | |||||||
| chr8:144310298 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.488+402G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310298 | |||||||
| chr8:144310335 | C | A | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.488+439C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310335 | |||||||
| chr8:144310459 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.488+563A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310459 | |||||||
| chr8:144310671 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.489-503G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310671 | |||||||
| chr8:144310674 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.489-500C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310674 | |||||||
| chr8:144310767 | C | T | 1 | a0001c0001t0008g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489-407C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310767 | |||||||
| chr8:144310941 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489-233C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310941 | |||||||
| chr8:144310969 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.489-205C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310969 | |||||||
| chr8:144310970 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0059 others(3): Show |
6 | HG01891.hp1 HG02300.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-204G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144310970 | |||||||
| chr8:144311007 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.489-167T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 4/12 | chr8 | 144311007 | |||||||
| chr8:144311289 | G | A | 1 | a0001c0001t0004g0135 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.565-32G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 5/12 | chr8 | 144311289 | |||||||
| chr8:144311416 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.626+34G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 6/12 | chr8 | 144311416 | |||||||
| chr8:144311455 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0009g0030 |
2 | HG02071.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.627-50C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 6/12 | chr8 | 144311455 | |||||||
| chr8:144311470 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.627-35G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 6/12 | chr8 | 144311470 | |||||||
| chr8:144311613 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.723+12A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 7/12 | chr8 | 144311613 | |||||||
| chr8:144311666 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.724-34C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 7/12 | chr8 | 144311666 | |||||||
| chr8:144311667 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.724-33G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 7/12 | chr8 | 144311667 | |||||||
| chr8:144311927 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861-36C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 8/12 | chr8 | 144311927 | |||||||
| chr8:144312370 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1142+126A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312370 | |||||||
| chr8:144312405 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1142+161G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312405 | |||||||
| chr8:144312460 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1142+216C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312460 | |||||||
| chr8:144312474 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+230C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312474 | |||||||
| chr8:144312475 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+231A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312475 | |||||||
| chr8:144312478 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+234C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312478 | |||||||
| chr8:144312479 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+235A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312479 | |||||||
| chr8:144312480 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+236C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312480 | |||||||
| chr8:144312481 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+237C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312481 | |||||||
| chr8:144312482 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+238C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312482 | |||||||
| chr8:144312483 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
116 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1142+239G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312483 | |||||||
| chr8:144312486 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+242C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312486 | |||||||
| chr8:144312487 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+243T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312487 | |||||||
| chr8:144312489 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+245C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312489 | |||||||
| chr8:144312490 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+246T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312490 | |||||||
| chr8:144312491 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+247G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312491 | |||||||
| chr8:144312493 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+249C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312493 | |||||||
| chr8:144312498 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+254C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312498 | |||||||
| chr8:144312504 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+260C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312504 | |||||||
| chr8:144312506 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+262A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312506 | |||||||
| chr8:144312508 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+264A>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312508 | |||||||
| chr8:144312516 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+272G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312516 | |||||||
| chr8:144312518 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+274C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312518 | |||||||
| chr8:144312522 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+278G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312522 | |||||||
| chr8:144312523 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+279G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312523 | |||||||
| chr8:144312524 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+280C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312524 | |||||||
| chr8:144312525 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+281A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312525 | |||||||
| chr8:144312526 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+282G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312526 | |||||||
| chr8:144312528 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+284T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312528 | |||||||
| chr8:144312532 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+288G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312532 | |||||||
| chr8:144312541 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+297A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312541 | |||||||
| chr8:144312553 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+309A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312553 | |||||||
| chr8:144312555 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+311A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312555 | |||||||
| chr8:144312556 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+312T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312556 | |||||||
| chr8:144312562 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+318G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312562 | |||||||
| chr8:144312564 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+320A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312564 | |||||||
| chr8:144312570 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+326G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312570 | |||||||
| chr8:144312572 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+328C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312572 | |||||||
| chr8:144312579 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1142+335A>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312579 | |||||||
| chr8:144312754 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0065 a0001c0001t0001g0121 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1142+510C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312754 | |||||||
| chr8:144312759 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0111 |
2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1142+515G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312759 | |||||||
| chr8:144312811 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
8 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1142+567C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312811 | |||||||
| chr8:144312821 | C | T | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1142+577C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312821 | |||||||
| chr8:144312907 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1143-604G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312907 | |||||||
| chr8:144312916 | G | A | 1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1143-595G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144312916 | |||||||
| chr8:144313067 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1143-444A>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144313067 | |||||||
| chr8:144313120 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1143-391C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144313120 | |||||||
| chr8:144313182 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1143-329G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144313182 | |||||||
| chr8:144313463 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1143-48G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | chr8 | 144313463 | |||||||
| chr8:144313491 | A | AC | 8 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0102 others(5): Show |
8 | HG00438.hp1 HG00735.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143-18dupC | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 144313491 | ||||||
| chr8:144313631 | G | GCCGCCCC others(6): Show |
2 | a0001c0001t0001g0037 a0001c0001t0009g0030 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1248+34_1248+46dup others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313631 | ||||||
| chr8:144313634 | G | GC | 4 | a0001c0001t0001g0066 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01192.hp1 NA18967.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+22dupC | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313634 | ||||||
| chr8:144313634 | G | GCCCCGCC others(24): Show |
1 | a0001c0001t0001g0258 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1248+25_1248+26ins others(31): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313634 | ||||||
| chr8:144313634 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1248+18G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313634 | |||||||
| chr8:144313635 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1248+19C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313635 | |||||||
| chr8:144313636 | CCCGCCTC others(22): Show |
C | 1 | a0001c0001t0001g0012 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1248+26_1248+54del others(29): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313636 | ||||||
| chr8:144313639 | G | GCCCCGCC others(3): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1248+25_1248+26ins others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313639 | ||||||
| chr8:144313639 | GCCTCCCC others(43): Show |
G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0071 |
3 | HG02109.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1248+26_1248+75del others(50): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313639 | ||||||
| chr8:144313642 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0141 others(3): Show |
6 | HG00621.hp1 HG02280.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+26T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313642 | |||||||
| chr8:144313642 | T | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1248+26T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313642 | |||||||
| chr8:144313644 | C | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0141 others(2): Show |
5 | HG00621.hp1 HG02280.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+28C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313644 | |||||||
| chr8:144313644 | CCCGCCCC others(14): Show |
C | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1248+47_1248+67del others(21): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313644 | ||||||
| chr8:144313647 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0214 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+31G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313647 | |||||||
| chr8:144313649 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1248+33C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313649 | |||||||
| chr8:144313649 | C | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02572.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1248+33C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313649 | |||||||
| chr8:144313650 | C | CCGCCCCG others(68): Show |
1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1248+38_1248+39ins others(75): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(3): Show |
115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1248+36_1248+45dup others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(21): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0160 others(3): Show |
7 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(89): Show |
1 | a0001c0001t0001g0171 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(96): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(89): Show |
19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(16): Show |
25 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(96): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(164): Show |
4 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0001g0212 others(1): Show |
4 | HG00438.hp1 NA18984.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(171): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(86): Show |
1 | a0001c0001t0001g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(93): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCCTCC others(107): Show |
1 | a0002c0002t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(114): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | C | CCGCGCCT others(81): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0214 |
2 | HG00621.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1248+37_1248+38ins others(88): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313650 | CCGCCTCC others(6): Show |
C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0127 |
4 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+39_1248+51del others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313650 | ||||||
| chr8:144313655 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1248+39T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313655 | |||||||
| chr8:144313655 | T | TCCCCGCG others(120): Show |
1 | a0002c0002t0001g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(127): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313655 | ||||||
| chr8:144313657 | CCCG | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0056 others(25): Show |
29 | HG00438.hp2 HG01243.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.1248+46_1248+48del others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313657 | ||||||
| chr8:144313657 | CCCGCCGC others(1): Show |
C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
8 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+47_1248+54del others(8): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313657 | ||||||
| chr8:144313658 | C | CCGCGCCT others(146): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0222 |
2 | HG01074.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(153): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313658 | ||||||
| chr8:144313658 | C | CCGCGCCT others(177): Show |
2 | a0001c0001t0001g0193 a0002c0002t0001g0173 |
2 | HG01255.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(184): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313658 | ||||||
| chr8:144313658 | C | CCGCGCCT others(156): Show |
1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(163): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313658 | ||||||
| chr8:144313660 | G | GCGCCTCC others(8): Show |
1 | a0001c0001t0001g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(15): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(21): Show |
2 | a0001c0001t0001g0110 a0001c0003t0001g0241 |
2 | HG02451.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(85): Show |
1 | a0001c0001t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(92): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(144): Show |
1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(151): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(68): Show |
1 | a0001c0001t0001g0233 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(75): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(175): Show |
1 | a0001c0001t0001g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(182): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(76): Show |
1 | a0001c0001t0001g0265 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(83): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(154): Show |
1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(161): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(146): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0261 |
2 | HG02738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(153): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(128): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0223 |
2 | HG02300.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(135): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(154): Show |
4 | a0001c0001t0001g0175 a0001c0001t0001g0210 a0001c0001t0002g0026 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(161): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(149): Show |
1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(156): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(141): Show |
1 | a0001c0001t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(148): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(154): Show |
4 | a0001c0001t0001g0156 a0001c0001t0001g0194 a0001c0001t0001g0211 others(1): Show |
4 | HG00323.hp2 HG02083.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(161): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(167): Show |
4 | a0001c0001t0001g0195 a0001c0001t0001g0204 a0001c0001t0001g0247 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(174): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(128): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0266 |
3 | HG02074.hp1 NA18953.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(135): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(180): Show |
1 | a0001c0001t0001g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(187): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(188): Show |
1 | a0001c0003t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(195): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(227): Show |
1 | a0001c0003t0001g0231 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(234): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(63): Show |
1 | a0001c0001t0001g0172 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(70): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(160): Show |
1 | a0001c0001t0001g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(167): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(94): Show |
9 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0001g0201 others(6): Show |
10 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(101): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(193): Show |
1 | a0002c0002t0001g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(200): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(138): Show |
1 | a0001c0001t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(145): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(112): Show |
1 | a0001c0001t0001g0182 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(119): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(86): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0158 others(1): Show |
6 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+45_1248+46ins others(93): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | G | GCGCCTCC others(77): Show |
1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1248+45_1248+46ins others(84): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | GCCGCGCC others(4): Show |
G | 1 | a0001c0001t0001g0019 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1248+46_1248+56del others(11): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313660 | GCCGCGCC others(38): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1248+46_1248+90del others(45): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313660 | ||||||
| chr8:144313663 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0007g0274 |
3 | HG01192.hp2 HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1248+47G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313663 | |||||||
| chr8:144313663 | G | GCAC | 3 | a0001c0001t0001g0110 a0001c0001t0001g0273 a0001c0003t0001g0241 |
3 | HG01884.hp1 HG02451.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1248+48_1248+49ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313663 | ||||||
| chr8:144313663 | G | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1248+47G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313663 | |||||||
| chr8:144313665 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1248+49G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313665 | |||||||
| chr8:144313665 | G | GCCTCCCC others(6): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0047 others(5): Show |
8 | HG00639.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+51_1248+52ins others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313665 | ||||||
| chr8:144313665 | G | GCCTCCCC others(228): Show |
1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+51_1248+52ins others(235): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313665 | ||||||
| chr8:144313665 | GCCGCCCC others(6): Show |
C | 1 | a0001c0001t0001g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1248+49_1248+61del others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313665 | |||||||
| chr8:144313668 | G | GCCT | 7 | a0001c0001t0001g0086 a0001c0001t0001g0193 a0001c0001t0001g0222 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+54_1248+55ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313668 | ||||||
| chr8:144313668 | G | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(51): Show |
61 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1248+52G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313668 | |||||||
| chr8:144313670 | C | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(55): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.1248+54C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313670 | |||||||
| chr8:144313670 | C | CCCGCCTC others(40): Show |
1 | a0001c0001t0001g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1248+66_1248+67ins others(47): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313670 | ||||||
| chr8:144313670 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1248+54C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313670 | |||||||
| chr8:144313671 | C | T | 24 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00323.hp2 HG01175.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1248+55C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313671 | |||||||
| chr8:144313673 | G | C | 24 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00323.hp2 HG01175.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1248+57G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313673 | |||||||
| chr8:144313676 | T | C | 1 | a0001c0006t0001g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1248+60T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313676 | |||||||
| chr8:144313676 | T | G | 24 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0149 others(21): Show |
24 | HG00323.hp2 HG01175.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1248+60T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313676 | |||||||
| chr8:144313676 | TCCCCG | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
106 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1248+68_1248+72del others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313676 | ||||||
| chr8:144313678 | C | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0149 others(22): Show |
25 | HG00323.hp2 HG01175.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248+62C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313678 | |||||||
| chr8:144313678 | CCCGCCCC others(22): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1248+81_1248+109de others(30): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313678 | ||||||
| chr8:144313681 | G | GCGCCGCC others(14): Show |
1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1248+66_1248+67ins others(21): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313681 | ||||||
| chr8:144313681 | G | T | 1 | a0001c0006t0001g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1248+65G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313681 | |||||||
| chr8:144313683 | C | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.1248+67C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | CCCGCCTC others(145): Show |
1 | a0001c0001t0001g0115 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1248+87_1248+88ins others(152): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313683 | ||||||
| chr8:144313683 | C | CCCGCCTC others(144): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0116 |
2 | NA18960.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1248+87_1248+88ins others(151): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313683 | ||||||
| chr8:144313683 | C | CTCCCCGC others(85): Show |
1 | a0001c0001t0001g0229 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1248+67_1248+68ins others(92): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | CTCCCCGC others(1): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0004c0007t0001g0129 |
3 | HG02300.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1248+67_1248+68ins others(8): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | CTCCCCGC others(22): Show |
1 | a0001c0001t0005g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1248+67_1248+68ins others(29): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | CTCCCCGC others(43): Show |
1 | a0001c0001t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1248+67_1248+68ins others(50): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | CTCCCCGC others(14): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0164 a0001c0001t0001g0181 others(4): Show |
10 | HG00558.hp2 HG00609.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1248+67_1248+68ins others(21): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313683 | C | G | 37 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0043 others(34): Show |
37 | HG00323.hp2 HG01074.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1248+67C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313683 | |||||||
| chr8:144313684 | C | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
6 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+68C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313684 | |||||||
| chr8:144313684 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0032 others(14): Show |
21 | HG00140.hp1 HG00621.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1248+68C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313684 | |||||||
| chr8:144313686 | G | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0032 others(14): Show |
21 | HG00140.hp1 HG00621.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1248+70G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313686 | |||||||
| chr8:144313689 | T | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(19): Show |
27 | HG00140.hp1 HG00621.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1248+73T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313689 | |||||||
| chr8:144313691 | C | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0141 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1248+75C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313691 | |||||||
| chr8:144313691 | C | CCCGCA | 5 | a0001c0001t0001g0198 a0001c0001t0001g0219 a0001c0001t0001g0244 others(2): Show |
5 | HG03017.hp1 HG03017.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+79_1248+80ins others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313691 | ||||||
| chr8:144313691 | C | CCCGCCTC others(6): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0145 |
2 | HG03471.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1248+87_1248+88ins others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313691 | ||||||
| chr8:144313691 | C | CCCGCCTC others(6): Show |
1 | a0001c0001t0001g0266 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1248+81_1248+93dup others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313691 | ||||||
| chr8:144313691 | C | CCCGCGCC others(11): Show |
1 | a0002c0002t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1248+79_1248+80ins others(18): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313691 | ||||||
| chr8:144313691 | C | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0032 others(12): Show |
19 | HG00621.hp1 HG01891.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1248+75C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313691 | |||||||
| chr8:144313692 | C | CCG | 4 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0127 others(1): Show |
9 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1248+78_1248+79dup others(2): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313692 | ||||||
| chr8:144313697 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0048 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1248+81T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313697 | |||||||
| chr8:144313697 | TCCCCGCG others(6): Show |
T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0089 |
2 | HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1248+88_1248+100de others(14): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313697 | ||||||
| chr8:144313699 | C | CCCGCACC others(144): Show |
1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1248+87_1248+88ins others(151): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313699 | ||||||
| chr8:144313699 | C | CCCGCACC others(50): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1248+87_1248+88ins others(57): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313699 | ||||||
| chr8:144313699 | C | CCCGCACC others(37): Show |
4 | a0001c0001t0001g0182 a0001c0001t0001g0217 a0002c0002t0001g0161 others(1): Show |
4 | HG02027.hp1 NA18988.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+87_1248+88ins others(44): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313699 | ||||||
| chr8:144313699 | C | CCCGCACC others(50): Show |
1 | a0001c0001t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1248+87_1248+88ins others(57): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313699 | ||||||
| chr8:144313699 | C | CCCGCACC others(76): Show |
1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1248+87_1248+88ins others(83): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313699 | ||||||
| chr8:144313699 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0099 |
3 | HG00280.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1248+83C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313699 | |||||||
| chr8:144313702 | G | GCCT | 2 | a0001c0001t0001g0005 a0001c0001t0001g0146 |
5 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+87_1248+88ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313702 | ||||||
| chr8:144313704 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(71): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.1248+88G>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313704 | |||||||
| chr8:144313704 | G | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(26): Show |
35 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1248+88G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313704 | |||||||
| chr8:144313704 | G | GCCGCCTC others(77): Show |
1 | a0001c0001t0001g0265 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1248+93_1248+94ins others(84): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313704 | ||||||
| chr8:144313705 | C | CCGCCTCC others(3): Show |
3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0273 |
3 | HG00140.hp2 HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1248+93_1248+94ins others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313705 | ||||||
| chr8:144313705 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1248+89C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313705 | |||||||
| chr8:144313705 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0001g0138 others(5): Show |
10 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+89C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313705 | |||||||
| chr8:144313705 | CCGCCGCC others(24): Show |
C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1248+94_1249-106de others(32): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313705 | ||||||
| chr8:144313707 | G | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0001g0138 others(5): Show |
10 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+91G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313707 | |||||||
| chr8:144313707 | G | GCCCCGCC others(3): Show |
1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1248+93_1248+94ins others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313707 | ||||||
| chr8:144313707 | G | GCCTCC | 10 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0153 others(7): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1248+93_1248+94ins others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313707 | ||||||
| chr8:144313707 | G | GCCTCCCC others(6): Show |
1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1248+93_1248+94ins others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313707 | ||||||
| chr8:144313707 | G | GCCTCCCC others(24): Show |
1 | a0002c0002t0001g0232 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1248+93_1248+94ins others(31): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313707 | ||||||
| chr8:144313707 | G | GCCTCCCC others(16): Show |
1 | a0001c0001t0001g0110 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1248+93_1248+94ins others(23): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313707 | ||||||
| chr8:144313710 | G | C | 1 | a0002c0002t0001g0069 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1248+94G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313710 | |||||||
| chr8:144313710 | G | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1248+94G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313710 | |||||||
| chr8:144313712 | C | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0130 a0001c0001t0001g0153 others(5): Show |
9 | HG02109.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1248+96C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313712 | |||||||
| chr8:144313712 | C | G | 9 | a0001c0001t0001g0044 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+96C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313712 | |||||||
| chr8:144313713 | CCGCCTCC others(16): Show |
C | 1 | a0001c0001t0001g0012 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1248+110_1249-98de others(24): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313713 | ||||||
| chr8:144313714 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0146 |
5 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+98C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313714 | |||||||
| chr8:144313717 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1248+101C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313717 | |||||||
| chr8:144313717 | C | G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0222 a0001c0001t0001g0256 others(2): Show |
5 | HG01099.hp1 HG01255.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+101C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313717 | |||||||
| chr8:144313718 | T | C | 10 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0151 others(7): Show |
10 | HG01099.hp1 HG01255.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+102T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313718 | |||||||
| chr8:144313718 | TCCCCG | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0035 others(6): Show |
11 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+110_1248+114d others(7): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313718 | ||||||
| chr8:144313719 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1248+103C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313719 | |||||||
| chr8:144313720 | C | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0151 others(6): Show |
9 | HG01099.hp1 HG01255.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1248+104C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313720 | |||||||
| chr8:144313721 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1248+105C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313721 | |||||||
| chr8:144313723 | G | GCACCGCC others(162): Show |
1 | a0002c0002t0001g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1248+108_1248+109i others(171): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCACCGCC others(131): Show |
1 | a0002c0002t0001g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1248+108_1248+109i others(140): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(157): Show |
1 | a0001c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(164): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(110): Show |
1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(117): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(97): Show |
1 | a0001c0001t0001g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(104): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(136): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0253 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1249-70_1249-69ins others(143): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(157): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0255 |
2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1249-70_1249-69ins others(164): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(123): Show |
1 | a0001c0001t0001g0234 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(130): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(118): Show |
16 | a0001c0001t0001g0021 a0001c0001t0001g0084 a0001c0001t0001g0094 others(13): Show |
17 | HG00099.hp1 HG00423.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1249-70_1249-69ins others(125): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(118): Show |
1 | a0001c0001t0001g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(125): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCCCGCC others(164): Show |
1 | a0001c0001t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1249-99_1249-98ins others(171): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0031 others(5): Show |
13 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1248+109_1248+110i others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCTCCCC others(100): Show |
2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1248+109_1248+110i others(109): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCCTCCCC others(85): Show |
1 | a0001c0001t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1248+109_1248+110i others(94): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCGCC others(1): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0182 others(7): Show |
11 | HG01081.hp2 HG01258.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+108_1248+109i others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCGCC others(45): Show |
1 | a0001c0001t0008g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1248+108_1248+109i others(54): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCGCC others(32): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0176 |
4 | HG01884.hp2 HG02818.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+108_1248+109i others(41): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCGCC others(19): Show |
1 | a0001c0001t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1248+108_1248+109i others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCGCC others(40): Show |
2 | a0001c0001t0001g0252 a0003c0004t0001g0028 |
3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1248+108_1248+109i others(49): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | GCGCCTCC others(30): Show |
1 | a0001c0001t0001g0147 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1248+108_1248+109i others(39): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313723 | ||||||
| chr8:144313723 | G | T | 10 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0151 others(7): Show |
10 | HG01099.hp1 HG01255.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+107G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313723 | |||||||
| chr8:144313725 | C | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0130 a0001c0001t0001g0233 others(1): Show |
4 | HG00597.hp1 HG02109.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+109C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313725 | |||||||
| chr8:144313725 | C | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(76): Show |
86 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1248+109C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313725 | |||||||
| chr8:144313726 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0096 others(3): Show |
6 | HG00438.hp2 HG04228.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+110C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313726 | |||||||
| chr8:144313726 | CCGCCTCC others(3): Show |
C | 13 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0056 others(10): Show |
13 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1249-108_1249-99de others(11): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313726 | ||||||
| chr8:144313728 | G | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0096 others(3): Show |
6 | HG00438.hp2 HG04228.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+112G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313728 | |||||||
| chr8:144313731 | T | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0096 others(3): Show |
6 | HG00438.hp2 HG04228.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+115T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313731 | |||||||
| chr8:144313733 | C | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0096 others(3): Show |
6 | HG00438.hp2 HG04228.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249-113C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313733 | |||||||
| chr8:144313734 | CCG | C | 29 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0039 others(26): Show |
29 | HG00323.hp2 HG00438.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1249-108_1249-107d others(4): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313734 | ||||||
| chr8:144313736 | G | GCCC | 7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0059 others(4): Show |
7 | HG02257.hp2 HG02300.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-109_1249-108i others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCCCGCC others(4): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0144 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1249-109_1249-108i others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCCCGCC others(105): Show |
1 | a0001c0001t0001g0233 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1249-109_1249-108i others(114): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCT | 5 | a0001c0001t0001g0099 a0001c0001t0001g0171 a0001c0001t0001g0177 others(2): Show |
5 | HG00280.hp2 HG01934.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-109_1249-108i others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCC | 3 | a0001c0001t0001g0141 a0001c0001t0002g0209 a0002c0002t0001g0173 |
3 | HG01255.hp1 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1249-109_1249-108i others(8): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCCC others(95): Show |
1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1249-109_1249-108i others(104): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCCC others(69): Show |
1 | a0001c0001t0001g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1249-109_1249-108i others(78): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCCC others(171): Show |
1 | a0001c0001t0001g0187 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1249-109_1249-108i others(180): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCCC others(4): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
17 | HG00621.hp1 HG01952.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1249-109_1249-108i others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCCTCCCC others(24): Show |
1 | a0001c0001t0001g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1249-109_1249-108i others(33): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGC | 44 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
53 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1249-108_1249-106d others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(4): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0158 others(3): Show |
8 | HG00558.hp2 HG00609.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-106_1249-105i others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(12): Show |
1 | a0001c0001t0001g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1249-106_1249-105i others(21): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(9): Show |
4 | a0001c0001t0001g0185 a0001c0001t0001g0252 a0001c0001t0001g0259 others(1): Show |
4 | HG00423.hp1 HG00642.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-106_1249-105i others(18): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(17): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0217 |
2 | HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1249-106_1249-105i others(26): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(30): Show |
1 | a0001c0001t0001g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1249-106_1249-105i others(39): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCC others(14): Show |
1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1249-106_1249-105i others(23): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | G | GCGCCGCG others(22): Show |
1 | a0001c0001t0001g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1249-106_1249-105i others(31): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313736 | GCGCCTCC others(42): Show |
G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0001g0098 others(2): Show |
5 | HG01081.hp1 HG02132.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-108_1249-60de others(50): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313736 | ||||||
| chr8:144313738 | G | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0171 a0001c0001t0001g0177 others(3): Show |
6 | HG00280.hp2 HG01358.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1249-108G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313738 | |||||||
| chr8:144313738 | GCCTCC | G | 11 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0166 others(8): Show |
12 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1249-105_1249-101d others(7): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313738 | ||||||
| chr8:144313738 | GCCTCCCC others(11): Show |
G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0071 |
3 | HG02109.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1249-105_1249-88de others(19): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313738 | ||||||
| chr8:144313739 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1249-107C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313739 | |||||||
| chr8:144313739 | CCTCCCCG others(3): Show |
C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
6 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249-105_1249-96de others(11): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313739 | ||||||
| chr8:144313741 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1249-105T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313741 | |||||||
| chr8:144313741 | T | G | 13 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0155 others(10): Show |
13 | HG00280.hp2 HG01081.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1249-105T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313741 | |||||||
| chr8:144313743 | C | CCCGCG | 6 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0141 others(3): Show |
6 | HG02129.hp1 HG02280.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249-99_1249-98ins others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313743 | ||||||
| chr8:144313743 | C | CTCCCCGC others(9): Show |
1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1249-103_1249-102i others(18): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313743 | |||||||
| chr8:144313743 | C | CTCCCCGC others(1): Show |
5 | a0001c0001t0001g0095 a0001c0001t0001g0184 a0001c0001t0001g0191 others(2): Show |
5 | HG01081.hp2 HG01192.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-103_1249-102i others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313743 | |||||||
| chr8:144313743 | C | CTCCCCGC others(14): Show |
1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1249-103_1249-102i others(23): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313743 | |||||||
| chr8:144313743 | C | CTCCCCGC others(27): Show |
1 | a0001c0001t0001g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1249-103_1249-102i others(36): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313743 | |||||||
| chr8:144313743 | C | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0171 a0001c0001t0001g0177 others(2): Show |
5 | HG00280.hp2 HG01934.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-103C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313743 | |||||||
| chr8:144313744 | C | CCG | 4 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0005g0046 others(1): Show |
4 | HG02257.hp2 HG02300.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-100_1249-99du others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313744 | ||||||
| chr8:144313748 | C | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0032 others(23): Show |
30 | HG00621.hp1 HG01074.hp2 HG01952.hp1 others(27): Show |
intron_variant | MODIFIER | c.1249-98C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313748 | |||||||
| chr8:144313749 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0032 others(25): Show |
32 | HG00621.hp1 HG01074.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-97T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313749 | |||||||
| chr8:144313749 | TCCCCG | T | 15 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0149 others(12): Show |
15 | HG01109.hp2 HG01515.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1249-89_1249-85del others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313749 | ||||||
| chr8:144313749 | TCCCCGCC others(32): Show |
T | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-89_1249-51del others(39): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313749 | ||||||
| chr8:144313751 | C | CCCGCCCC others(121): Show |
1 | a0001c0001t0001g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1249-70_1249-69ins others(128): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313751 | ||||||
| chr8:144313751 | C | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0021 others(30): Show |
38 | HG00621.hp1 HG01074.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1249-95C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313751 | |||||||
| chr8:144313753 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1249-93C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313753 | |||||||
| chr8:144313754 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1249-92G>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313754 | |||||||
| chr8:144313754 | G | GCCT | 37 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
42 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1249-90_1249-89ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313754 | ||||||
| chr8:144313754 | G | GCGCCGCC others(14): Show |
2 | a0001c0001t0001g0172 a0002c0002t0001g0232 |
2 | HG01978.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1249-91_1249-90ins others(21): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313754 | ||||||
| chr8:144313754 | G | GCGCCGCC others(22): Show |
1 | a0001c0001t0008g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1249-91_1249-90ins others(29): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313754 | ||||||
| chr8:144313754 | G | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0032 others(23): Show |
30 | HG00621.hp1 HG01074.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1249-92G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313754 | |||||||
| chr8:144313756 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1249-90C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313756 | |||||||
| chr8:144313756 | C | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1249-90C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313756 | |||||||
| chr8:144313765 | C | CCG | 4 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0151 others(1): Show |
4 | HG02300.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-79_1249-78dup others(2): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313765 | ||||||
| chr8:144313769 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1249-77C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313769 | |||||||
| chr8:144313770 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1249-76T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313770 | |||||||
| chr8:144313770 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1249-76T>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313770 | |||||||
| chr8:144313770 | TCCCCGCC others(11): Show |
T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0109 a0001c0001t0006g0049 |
3 | HG02486.hp2 HG02602.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1249-68_1249-51del others(18): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313770 | ||||||
| chr8:144313772 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0224 |
2 | HG03471.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1249-74C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313772 | |||||||
| chr8:144313775 | G | GCCT | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(71): Show |
85 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1249-69_1249-68ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | GCCTCCCC others(12): Show |
1 | a0002c0002t0001g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1249-69_1249-68ins others(19): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | GCCTCCCC others(4): Show |
3 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0249 |
3 | HG00140.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1249-69_1249-68ins others(11): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | GCCTCCCC others(20): Show |
1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1249-69_1249-68ins others(27): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | GCCTCCCC others(28): Show |
1 | a0001c0001t0001g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1249-69_1249-68ins others(35): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | GCCTCCCC others(17): Show |
1 | a0001c0001t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1249-69_1249-68ins others(24): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | G | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02572.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-71G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313775 | |||||||
| chr8:144313775 | GCC | G | 20 | a0001c0001t0001g0057 a0001c0001t0001g0086 a0001c0001t0001g0166 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1249-68_1249-67del others(2): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313775 | GCCCCGCC others(3): Show |
G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0052 others(5): Show |
8 | HG01884.hp2 HG01975.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-68_1249-59del others(10): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313775 | ||||||
| chr8:144313777 | C | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0045 others(25): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1249-69C>A | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313777 | |||||||
| chr8:144313777 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
139 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1249-69C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313777 | |||||||
| chr8:144313780 | G | T | 20 | a0001c0001t0001g0057 a0001c0001t0001g0086 a0001c0001t0001g0166 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1249-66G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313780 | |||||||
| chr8:144313783 | T | C | 20 | a0001c0001t0001g0057 a0001c0001t0001g0086 a0001c0001t0001g0166 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1249-63T>C | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313783 | |||||||
| chr8:144313783 | TCCCCG | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0071 others(2): Show |
7 | HG02109.hp2 HG02145.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1249-55_1249-51del others(5): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313783 | ||||||
| chr8:144313785 | C | G | 20 | a0001c0001t0001g0057 a0001c0001t0001g0086 a0001c0001t0001g0166 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1249-61C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313785 | |||||||
| chr8:144313788 | G | GCACCGCC others(132): Show |
1 | a0001c0001t0007g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(139): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCACCGCC others(108): Show |
1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(115): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCACCGCC others(161): Show |
1 | a0001c0003t0001g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(168): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCACCGCC others(124): Show |
1 | a0001c0001t0001g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(131): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCCT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1249-56_1249-55ins others(3): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCCTCCCC others(156): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1249-56_1249-55ins others(163): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCCTCCCC others(40): Show |
1 | a0001c0001t0001g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1249-56_1249-55ins others(47): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCCTCCCC others(48): Show |
1 | a0001c0001t0001g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1249-56_1249-55ins others(55): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCCTCCCC others(135): Show |
1 | a0001c0001t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1249-56_1249-55ins others(142): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(6): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1249-57_1249-56ins others(13): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(201): Show |
1 | a0001c0001t0001g0160 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(208): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(9): Show |
1 | a0001c0001t0001g0233 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(16): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(318): Show |
1 | a0001c0001t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(325): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(252): Show |
1 | a0001c0001t0001g0228 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(259): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(93): Show |
1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(100): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(157): Show |
1 | a0001c0001t0001g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(164): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(96): Show |
1 | a0001c0001t0001g0229 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(103): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(120): Show |
1 | a0001c0001t0001g0003 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(127): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(136): Show |
1 | a0001c0001t0001g0174 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(143): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(144): Show |
1 | a0001c0001t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(151): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(107): Show |
1 | a0002c0002t0001g0069 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(114): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(96): Show |
1 | a0002c0002t0001g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(103): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(117): Show |
1 | a0001c0001t0001g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(124): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(200): Show |
1 | a0001c0001t0001g0240 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(207): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(166): Show |
1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(173): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(407): Show |
1 | a0001c0001t0001g0219 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(414): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(210): Show |
1 | a0001c0001t0001g0022 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(217): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(321): Show |
1 | a0001c0001t0001g0198 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(328): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(90): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0168 |
2 | NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1249-57_1249-56ins others(97): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(108): Show |
1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(115): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(238): Show |
1 | a0001c0001t0001g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(245): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(208): Show |
1 | a0001c0001t0001g0226 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(215): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(310): Show |
1 | a0001c0001t0001g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(317): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(109): Show |
1 | a0001c0001t0001g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(116): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(132): Show |
1 | a0001c0001t0001g0064 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(139): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(333): Show |
1 | a0001c0001t0001g0243 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(340): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(177): Show |
1 | a0001c0001t0001g0258 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(184): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(243): Show |
1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(250): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(248): Show |
1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(255): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(289): Show |
1 | a0001c0001t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(296): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(435): Show |
1 | a0001c0001t0001g0242 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(442): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(295): Show |
1 | a0001c0001t0001g0244 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(302): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(185): Show |
1 | a0001c0001t0001g0003 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(192): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(265): Show |
1 | a0001c0001t0001g0003 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(272): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(300): Show |
1 | a0001c0001t0001g0263 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(307): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(151): Show |
1 | a0001c0001t0001g0003 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(158): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCC others(305): Show |
1 | a0001c0001t0001g0203 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(312): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCG others(141): Show |
1 | a0001c0001t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(148): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | GCGCCGCG others(367): Show |
1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1249-57_1249-56ins others(374): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313788 | ||||||
| chr8:144313788 | G | T | 34 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0051 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1249-58G>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313788 | |||||||
| chr8:144313795 | C | CTCCCCGC others(30): Show |
1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1249-43_1249-42ins others(37): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313795 | ||||||
| chr8:144313795 | C | CTCCCCGC others(27): Show |
2 | a0001c0001t0001g0045 a0001c0001t0005g0046 |
2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1249-44_1249-43ins others(34): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313795 | ||||||
| chr8:144313795 | C | CTCCCCGC others(19): Show |
1 | a0004c0007t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1249-44_1249-43ins others(26): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313795 | ||||||
| chr8:144313795 | C | CTCCCCGC others(388): Show |
1 | a0001c0001t0009g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1249-44_1249-43ins others(395): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 144313795 | ||||||
| chr8:144313795 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1249-51C>T | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313795 | |||||||
| chr8:144313803 | C | G | 1 | a0001c0009t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-43C>G | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | chr8 | 144313803 | |||||||
| chr8:144314109 | A | AC | 9 | a0001c0001t0001g0063 a0001c0001t0001g0092 a0001c0001t0001g0103 others(6): Show |
9 | HG00438.hp1 HG00438.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1385-11dupC | HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 144314109 |