Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10808 |
| ensemblid | ENSG00000120694.20 |
| hgncid | 16969 |
| symbol | HSPH1 |
| name | heat shock protein family H (Hsp110) member 1 |
| refseq_nuc | NM_006644.4 |
| refseq_prot | NP_006635.2 |
| ensembl_nuc | ENST00000320027.10 |
| ensembl_prot | ENSP00000318687.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 31134973 |
| end | 31161904 |
| strand | - |
| ver | v1.2 |
| region | chr13:31134973-31161904 |
| region5000 | chr13:31129973-31166904 |
| regionname0 | HSPH1_chr13_31134973_31161904 |
| regionname5000 | HSPH1_chr13_31129973_31166904 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 858 | 388 | 88 | 72 | 172 | 18 | 36 | 128 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| a0002 | 0/0 | 858 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| a0003 | 0/0 | 858 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| a0004 | 0/0 | 858 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| a0005 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| a0006 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | MSVVG others(853): Show |
chr13 | 31129973 | 31166904 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2574 | 325 | 67 | 49 | 167 | 11 | 29 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0002 | 0/0 | 2574 | 51 | 17 | 17 | 3 | 7 | 7 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0003 | 0/0 | 2574 | 6 | 0 | 6 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0006 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0007 | 0/0 | 2574 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0008 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0001c0010 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0002c0004 | 0/0 | 2574 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0003c0005 | 0/0 | 2574 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0004c0012 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0005c0009 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 | ||
| a0006c0011 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | ATGTC others(2569): Show |
chr13 | 31129973 | 31166904 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5244 | 121 | 11 | 17 | 75 | 2 | 16 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0002 | 0/1 | 5244 | 80 | 5 | 17 | 47 | 5 | 5 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0004 | 0/0 | 5244 | 41 | 19 | 7 | 7 | 2 | 6 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0005 | 1/0 | 5244 | 41 | 4 | 4 | 28 | 2 | 2 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0006 | 0/0 | 5242 | 14 | 13 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0007 | 0/0 | 5244 | 6 | 5 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0008 | 0/0 | 5242 | 5 | 5 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0009 | 0/0 | 5242 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0011 | 0/0 | 5242 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0012 | 0/0 | 5244 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0013 | 0/0 | 5242 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0015 | 0/0 | 5242 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0016 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0017 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0020 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0022 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0023 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0001t0024 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0002t0003 | 0/0 | 5244 | 49 | 15 | 17 | 3 | 7 | 7 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0002t0018 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0002t0019 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0003t0001 | 0/0 | 5244 | 6 | 0 | 6 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0006t0014 | 0/0 | 5244 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0007t0001 | 0/0 | 5244 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0001c0008t0006 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0001c0010t0025 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0002c0004t0010 | 0/0 | 5238 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5233): Show |
chr13 | 31129973 | 31166904 |
| a0003c0005t0001 | 0/0 | 5244 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0004c0012t0021 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5237): Show |
chr13 | 31129973 | 31166904 |
| a0005c0009t0001 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| a0006c0011t0001 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | GGGTC others(5239): Show |
chr13 | 31129973 | 31166904 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 35 | 0 | 3 | 24 | 0 | 8 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0002 | 0/0 | 33 | 0 | 2 | 29 | 0 | 2 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0008 | 0/0 | 7 | 3 | 3 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0005 | 0/0 | 15 | 6 | 0 | 3 | 2 | 4 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0003 | 1/0 | 20 | 3 | 1 | 13 | 2 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0007g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0008g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0011g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0016g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0017g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0020g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0023g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0001t0024g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0004 | 0/0 | 18 | 5 | 6 | 0 | 4 | 3 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0010 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0002t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0003t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0006t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0006t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0008t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0001c0010t0025g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0002c0004t0010g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0003c0005t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0004c0012t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0005c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| a0006c0011t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | GBR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | GBR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0010 | EUR | GBR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0005 | EUR | GBR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | FIN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | FIN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0152 | EUR | FIN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00738 | hp1 | a0001 | c0001 | t0012 | g0051 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0148 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0040 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0183 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0074 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01256 | hp1 | a0003 | c0005 | t0001 | g0027 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01346 | hp1 | a0003 | c0005 | t0001 | g0027 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0145 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0133 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0144 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02055 | hp1 | a0001 | c0002 | t0019 | g0150 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0140 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0138 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0047 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CDX | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0135 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0155 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02451 | hp1 | a0002 | c0004 | t0010 | g0022 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0190 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02717 | hp2 | a0004 | c0012 | t0021 | g0086 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02723 | hp1 | a0001 | c0006 | t0014 | g0187 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0189 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0154 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0191 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0076 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0095 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0143 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0188 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03098 | hp2 | a0002 | c0004 | t0010 | g0022 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03195 | hp1 | a0002 | c0004 | t0010 | g0022 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03195 | hp2 | a0001 | c0008 | t0006 | g0093 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0040 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03453 | hp2 | a0001 | c0002 | t0018 | g0139 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | ESN | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0146 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0114 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0041 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0117 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | YRI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18941 | hp2 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18944 | hp2 | a0001 | c0007 | t0001 | g0075 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18952 | hp1 | a0001 | c0001 | t0020 | g0072 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18963 | hp2 | a0001 | c0001 | t0024 | g0168 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18980 | hp1 | a0001 | c0001 | t0016 | g0104 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18990 | hp1 | a0001 | c0001 | t0023 | g0088 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18997 | hp2 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19003 | hp2 | a0005 | c0009 | t0001 | g0060 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19010 | hp2 | a0001 | c0007 | t0001 | g0057 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19055 | hp2 | a0006 | c0011 | t0001 | g0085 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19074 | hp1 | a0001 | c0001 | t0017 | g0105 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19081 | hp2 | a0001 | c0001 | t0013 | g0130 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19086 | hp2 | a0001 | c0001 | t0022 | g0073 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | YRI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | YRI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ASW | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ASW | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0134 | EUR | TSI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0005 | EUR | TSI | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0136 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0156 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0041 | AFR | USA | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | USA | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20300 | hp1 | a0001 | c0006 | t0014 | g0186 | AFR | USA | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | USA | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA21309 | hp1 | a0001 | c0010 | t0025 | g0163 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | LWK | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0179 | REF | REF | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0003 | REF | REF | HSPH1_chr13_31129973_31166904 | HSPH1 | chr13 | 31129973 | 31166904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31145563 | A | C | 1 | a0002 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1584T>G | p.Asp528Glu | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/18 | 1906/5244 | 1584/2577 | 528/858 | chr13 | 31145563 | |||
| chr13:31148034 | G | C | 1 | a0003 | 2 | HG01256.hp1 HG01346.hp1 |
missense_variant | MODERATE | c.1303C>G | p.Leu435Val | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/18 | 1625/5244 | 1303/2577 | 435/858 | chr13 | 31148034 | |||
| chr13:31151098 | T | C | 1 | a0006 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.757A>G | p.Lys253Glu | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/18 | 1079/5244 | 757/2577 | 253/858 | chr13 | 31151098 | |||
| chr13:31151118 | G | C | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.737C>G | p.Ala246Gly | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/18 | 1059/5244 | 737/2577 | 246/858 | chr13 | 31151118 | |||
| chr13:31152915 | C | T | 1 | a0005 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.466G>A | p.Val156Met | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/18 | 788/5244 | 466/2577 | 156/858 | chr13 | 31152915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31137501 | G | A | 1 | a0001c0007 | 2 | NA18944.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.2394C>T | p.Pro798Pro | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 2716/5244 | 2394/2577 | 798/858 | chr13 | 31137501 | |||
| chr13:31139036 | A | G | 1 | a0001c0006 | 2 | HG02723.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2052T>C | p.Ala684Ala | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 15/18 | 2374/5244 | 2052/2577 | 684/858 | chr13 | 31139036 | |||
| chr13:31139084 | G | C | 1 | a0001c0006 | 2 | HG02723.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2004C>G | p.Leu668Leu | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 15/18 | 2326/5244 | 2004/2577 | 668/858 | chr13 | 31139084 | |||
| chr13:31150134 | T | C | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.957A>G | p.Val319Val | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/18 | 1279/5244 | 957/2577 | 319/858 | chr13 | 31150134 | |||
| chr13:31151123 | A | G | 2 | a0001c0002 a0001c0006 |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
synonymous_variant | LOW | c.732T>C | p.Phe244Phe | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/18 | 1054/5244 | 732/2577 | 244/858 | chr13 | 31151123 | |||
| chr13:31155574 | C | T | 1 | a0001c0008 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.246G>A | p.Lys82Lys | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/18 | 568/5244 | 246/2577 | 82/858 | chr13 | 31155574 | |||
| chr13:31155592 | A | G | 2 | a0001c0002 a0001c0006 |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
synonymous_variant | LOW | c.228T>C | p.Asn76Asn | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/18 | 550/5244 | 228/2577 | 76/858 | chr13 | 31155592 | |||
| chr13:31161538 | G | T | 2 | a0001c0003 a0003c0005 |
8 | HG01192.hp1 HG01256.hp1 HG01346.hp1 others(5): Show |
synonymous_variant | LOW | c.45C>A | p.Ile15Ile | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/18 | 367/5244 | 45/2577 | 15/858 | chr13 | 31161538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31135139 | T | C | 1 | a0001c0001t0009 | 3 | HG02630.hp2 HG03139.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2179A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 2179 | chr13 | 31135139 | ||||||
| chr13:31135179 | C | T | 1 | a0001c0001t0022 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2139G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 2139 | chr13 | 31135179 | ||||||
| chr13:31135191 | C | T | 4 | a0001c0001t0006 a0001c0001t0009 a0001c0008t0006 others(1): Show |
19 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2127G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 2127 | chr13 | 31135191 | ||||||
| chr13:31135281 | TCA | T | 9 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(6): Show |
33 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2035_*2036delTG | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 2035 | chr13 | 31135281 | ||||||
| chr13:31135455 | T | C | 2 | a0001c0002t0018 a0001c0002t0019 |
2 | HG02055.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1863A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1863 | chr13 | 31135455 | ||||||
| chr13:31135472 | A | G | 1 | a0001c0001t0016 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1846 | chr13 | 31135472 | ||||||
| chr13:31135523 | TAGTA | T | 1 | a0002c0004t0010 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1791_*1794delTACT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1791 | chr13 | 31135523 | ||||||
| chr13:31135541 | T | G | 1 | a0004c0012t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1777A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1777 | chr13 | 31135541 | ||||||
| chr13:31135546 | A | G | 1 | a0004c0012t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1772T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1772 | chr13 | 31135546 | ||||||
| chr13:31135572 | T | C | 1 | a0001c0001t0013 | 2 | NA18997.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1746A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1746 | chr13 | 31135572 | ||||||
| chr13:31135669 | A | C | 3 | a0001c0002t0003 a0001c0002t0018 a0001c0002t0019 |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1649T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1649 | chr13 | 31135669 | ||||||
| chr13:31135742 | A | G | 1 | a0001c0002t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1576T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1576 | chr13 | 31135742 | ||||||
| chr13:31135883 | T | A | 10 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0020 others(7): Show |
138 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1435A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1435 | chr13 | 31135883 | ||||||
| chr13:31135994 | C | T | 1 | a0001c0001t0020 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1324 | chr13 | 31135994 | ||||||
| chr13:31136023 | A | G | 1 | a0001c0001t0024 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1295T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1295 | chr13 | 31136023 | ||||||
| chr13:31136044 | A | C | 3 | a0001c0002t0003 a0001c0002t0018 a0001c0002t0019 |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1274T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1274 | chr13 | 31136044 | ||||||
| chr13:31136186 | T | C | 1 | a0001c0001t0012 | 2 | HG00738.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1132 | chr13 | 31136186 | ||||||
| chr13:31136218 | C | T | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1100G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 1100 | chr13 | 31136218 | ||||||
| chr13:31136397 | G | A | 1 | a0001c0001t0023 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*921C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 921 | chr13 | 31136397 | ||||||
| chr13:31136524 | A | T | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | NA18980.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 794 | chr13 | 31136524 | ||||||
| chr13:31136833 | G | A | 1 | a0001c0001t0007 | 6 | HG01175.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*485C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 485 | chr13 | 31136833 | ||||||
| chr13:31136858 | G | A | 1 | a0001c0001t0013 | 2 | NA18997.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*460C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 460 | chr13 | 31136858 | ||||||
| chr13:31137070 | G | A | 1 | a0001c0010t0025 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 18/18 | 248 | chr13 | 31137070 | ||||||
| chr13:31161622 | G | A | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(4): Show |
97 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/18 | 40 | chr13 | 31161622 | ||||||
| chr13:31161665 | G | A | 1 | a0001c0006t0014 | 2 | HG02723.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-83C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/18 | 83 | chr13 | 31161665 | ||||||
| chr13:31161748 | C | A | 2 | a0001c0001t0008 a0001c0001t0015 |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/18 | 166 | chr13 | 31161748 | ||||||
| chr13:31161828 | G | C | 1 | a0001c0001t0008 | 5 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-246C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/18 | 246 | chr13 | 31161828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31137562 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2371-38T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137562 | |||||||
| chr13:31137615 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2371-91G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137615 | |||||||
| chr13:31137668 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2371-144G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137668 | |||||||
| chr13:31137720 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
196 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.2371-196A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137720 | |||||||
| chr13:31137826 | A | T | 22 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0052 others(19): Show |
30 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.2371-302T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137826 | |||||||
| chr13:31137906 | G | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2371-382C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137906 | |||||||
| chr13:31137930 | T | C | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2371-406A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31137930 | |||||||
| chr13:31138013 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2370+394G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31138013 | |||||||
| chr13:31138015 | T | C | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2370+392A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31138015 | |||||||
| chr13:31138048 | C | T | 15 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0052 others(12): Show |
19 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2370+359G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31138048 | |||||||
| chr13:31138107 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0089 |
5 | NA18968.hp2 NA18977.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2370+300C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31138107 | |||||||
| chr13:31138112 | A | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0128 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2370+295T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 17/17 | chr13 | 31138112 | |||||||
| chr13:31138760 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2208+21A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 16/17 | chr13 | 31138760 | |||||||
| chr13:31138928 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2089-28A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 15/17 | chr13 | 31138928 | |||||||
| chr13:31138993 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.2088+7C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 15/17 | chr13 | 31138993 | |||||||
| chr13:31139191 | T | C | 1 | a0001c0001t0006g0095 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1981-84A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139191 | |||||||
| chr13:31139315 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1981-208C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139315 | |||||||
| chr13:31139385 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
145 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1981-278A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139385 | |||||||
| chr13:31139405 | A | T | 14 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0046 others(11): Show |
27 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1981-298T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139405 | |||||||
| chr13:31139461 | C | T | 1 | a0001c0001t0006g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1981-354G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139461 | |||||||
| chr13:31139587 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1981-480G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139587 | |||||||
| chr13:31139647 | T | C | 1 | a0001c0001t0008g0026 | 3 | HG02280.hp2 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1980+537A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139647 | |||||||
| chr13:31139703 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1980+481C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139703 | |||||||
| chr13:31139731 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1980+453C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139731 | |||||||
| chr13:31139850 | C | A | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1980+334G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31139850 | |||||||
| chr13:31140006 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1980+178A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31140006 | |||||||
| chr13:31140034 | C | T | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1980+150G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31140034 | |||||||
| chr13:31140044 | C | T | 1 | a0001c0002t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1980+140G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 14/17 | chr13 | 31140044 | |||||||
| chr13:31140425 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1855-116G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140425 | |||||||
| chr13:31140553 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
167 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.1855-245dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140553 | |||||||
| chr13:31140553 | T | TAA | 25 | a0001c0001t0001g0030 a0001c0001t0001g0082 a0001c0001t0006g0076 others(22): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1855-246_1855-245d others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140553 | |||||||
| chr13:31140624 | A | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1855-315T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140624 | |||||||
| chr13:31140685 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0100 |
3 | HG02055.hp2 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1855-376T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140685 | |||||||
| chr13:31140738 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0178 a0001c0001t0002g0184 |
7 | HG00735.hp1 HG01167.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+384C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140738 | |||||||
| chr13:31140766 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1854+356A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140766 | |||||||
| chr13:31140784 | T | C | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1854+338A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140784 | |||||||
| chr13:31140878 | T | C | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1854+244A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31140878 | |||||||
| chr13:31141088 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1854+34A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 13/17 | chr13 | 31141088 | |||||||
| chr13:31141302 | C | T | 7 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(4): Show |
11 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1717-43G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141302 | |||||||
| chr13:31141318 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1717-59T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141318 | |||||||
| chr13:31141418 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
168 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.1717-159A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141418 | |||||||
| chr13:31141489 | AT | A | 1 | a0001c0001t0006g0018 | 3 | HG02630.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1717-231delA | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141489 | |||||||
| chr13:31141522 | G | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1717-263C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141522 | |||||||
| chr13:31141539 | A | G | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1717-280T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141539 | |||||||
| chr13:31141683 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1717-424T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141683 | |||||||
| chr13:31141749 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1717-490T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141749 | |||||||
| chr13:31141760 | T | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1717-501A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141760 | |||||||
| chr13:31141793 | CACAT | C | 3 | a0001c0001t0001g0064 a0001c0002t0003g0135 a0001c0002t0003g0151 |
3 | HG01109.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1717-538_1717-535d others(6): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141793 | |||||||
| chr13:31141797 | T | TAC | 14 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0058 others(11): Show |
21 | HG00609.hp1 HG01106.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1717-540_1717-539d others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141797 | |||||||
| chr13:31141797 | T | TACAC | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(54): Show |
110 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1717-539_1717-538i others(6): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141797 | |||||||
| chr13:31141797 | T | TACACAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0030 others(7): Show |
19 | HG00544.hp1 HG02451.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1717-539_1717-538i others(8): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141797 | |||||||
| chr13:31141797 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0056 others(3): Show |
9 | HG01928.hp2 HG02015.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-539_1717-538i others(10): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141797 | |||||||
| chr13:31141797 | TACATACA others(1): Show |
T | 8 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0002t0003g0010 others(5): Show |
12 | HG00140.hp1 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1717-546_1717-539d others(10): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141797 | |||||||
| chr13:31141799 | CAT | C | 25 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0128 others(22): Show |
45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1717-542_1717-541d others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141799 | |||||||
| chr13:31141801 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
168 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.1717-542A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141801 | |||||||
| chr13:31141801 | T | TAC | 18 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0042 others(15): Show |
56 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1717-544_1717-543d others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141801 | |||||||
| chr13:31141807 | C | T | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1717-548G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141807 | |||||||
| chr13:31141869 | A | G | 1 | a0001c0001t0002g0023 | 3 | NA18747.hp1 NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1717-610T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141869 | |||||||
| chr13:31141876 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1717-617A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141876 | |||||||
| chr13:31141900 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1717-641A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141900 | |||||||
| chr13:31141985 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1717-726T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31141985 | |||||||
| chr13:31142066 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1717-807T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142066 | |||||||
| chr13:31142094 | T | A | 1 | a0001c0002t0003g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1717-835A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142094 | |||||||
| chr13:31142171 | C | T | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1717-912G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142171 | |||||||
| chr13:31142310 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1717-1051C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142310 | |||||||
| chr13:31142658 | G | C | 7 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(4): Show |
11 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+1134C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142658 | |||||||
| chr13:31142749 | T | C | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1716+1043A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142749 | |||||||
| chr13:31142769 | T | C | 1 | a0001c0001t0005g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1716+1023A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142769 | |||||||
| chr13:31142939 | T | C | 1 | a0001c0003t0001g0047 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1716+853A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31142939 | |||||||
| chr13:31143021 | T | C | 1 | a0001c0001t0006g0096 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1716+771A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31143021 | |||||||
| chr13:31143416 | T | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1716+376A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31143416 | |||||||
| chr13:31143690 | G | A | 1 | a0001c0001t0009g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1716+102C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31143690 | |||||||
| chr13:31143698 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1716+94A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 12/17 | chr13 | 31143698 | |||||||
| chr13:31144088 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1585-165G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144088 | |||||||
| chr13:31144415 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1585-492G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144415 | |||||||
| chr13:31144587 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1585-664G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144587 | |||||||
| chr13:31144675 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1585-752G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144675 | |||||||
| chr13:31144839 | A | C | 1 | a0001c0001t0007g0175 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1584+724T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144839 | |||||||
| chr13:31144890 | G | C | 1 | a0001c0001t0002g0170 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1584+673C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144890 | |||||||
| chr13:31144991 | T | C | 30 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(27): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.1584+572A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144991 | |||||||
| chr13:31144993 | G | T | 1 | a0001c0002t0003g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1584+570C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31144993 | |||||||
| chr13:31145002 | T | C | 1 | a0001c0001t0005g0119 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1584+561A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31145002 | |||||||
| chr13:31145132 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1584+431A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31145132 | |||||||
| chr13:31145144 | C | A | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0083 |
3 | HG02630.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1584+419G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31145144 | |||||||
| chr13:31145189 | A | G | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1584+374T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 11/17 | chr13 | 31145189 | |||||||
| chr13:31145872 | C | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1379-104G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31145872 | |||||||
| chr13:31146007 | C | T | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1379-239G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146007 | |||||||
| chr13:31146029 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1379-261C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146029 | |||||||
| chr13:31146185 | AC | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0035 |
6 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-418delG | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146185 | |||||||
| chr13:31146234 | A | G | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-466T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146234 | |||||||
| chr13:31146269 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-501A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146269 | |||||||
| chr13:31146280 | T | A | 1 | a0001c0006t0014g0187 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1379-512A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146280 | |||||||
| chr13:31146397 | A | G | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1379-629T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146397 | |||||||
| chr13:31146837 | G | C | 1 | a0001c0001t0004g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1379-1069C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146837 | |||||||
| chr13:31146846 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1379-1078T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31146846 | |||||||
| chr13:31147025 | T | G | 1 | a0001c0002t0003g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1378+934A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147025 | |||||||
| chr13:31147083 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1378+876G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147083 | |||||||
| chr13:31147118 | A | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1378+841T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147118 | |||||||
| chr13:31147368 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+591A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147368 | |||||||
| chr13:31147433 | AAG | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1378+524_1378+525d others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147433 | |||||||
| chr13:31147502 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378+457T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147502 | |||||||
| chr13:31147555 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+404A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147555 | |||||||
| chr13:31147560 | G | A | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+399C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147560 | |||||||
| chr13:31147569 | G | A | 5 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0144 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+390C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147569 | |||||||
| chr13:31147609 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1378+350A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 10/17 | chr13 | 31147609 | |||||||
| chr13:31148240 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1244+134A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 9/17 | chr13 | 31148240 | |||||||
| chr13:31148483 | TA | T | 32 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(29): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1138-4delT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148483 | |||||||
| chr13:31148560 | G | A | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1138-80C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148560 | |||||||
| chr13:31148572 | C | CA | 28 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(25): Show |
80 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1138-93dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148572 | |||||||
| chr13:31148572 | CA | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
160 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1138-93delT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148572 | |||||||
| chr13:31148572 | CAA | C | 33 | a0001c0001t0004g0125 a0001c0001t0004g0126 a0001c0001t0006g0062 others(30): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1138-94_1138-93del others(2): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148572 | |||||||
| chr13:31148613 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1138-133A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148613 | |||||||
| chr13:31148693 | A | G | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1138-213T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148693 | |||||||
| chr13:31148731 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1138-251G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148731 | |||||||
| chr13:31148981 | C | T | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1138-501G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148981 | |||||||
| chr13:31148993 | G | A | 1 | a0001c0001t0009g0083 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1138-513C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31148993 | |||||||
| chr13:31149028 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1138-548T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149028 | |||||||
| chr13:31149036 | C | T | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1138-556G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149036 | |||||||
| chr13:31149114 | A | C | 1 | a0001c0001t0004g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1138-634T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149114 | |||||||
| chr13:31149379 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137+575A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149379 | |||||||
| chr13:31149508 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1137+446C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149508 | |||||||
| chr13:31149509 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1137+445G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149509 | |||||||
| chr13:31149536 | A | G | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1137+418T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149536 | |||||||
| chr13:31149574 | T | C | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1137+380A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149574 | |||||||
| chr13:31149722 | T | C | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1137+232A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 8/17 | chr13 | 31149722 | |||||||
| chr13:31150373 | G | A | 1 | a0001c0001t0006g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.909-191C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/17 | chr13 | 31150373 | |||||||
| chr13:31150374 | G | C | 1 | a0001c0001t0004g0121 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.909-192C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/17 | chr13 | 31150374 | |||||||
| chr13:31150445 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.909-263T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/17 | chr13 | 31150445 | |||||||
| chr13:31150664 | T | G | 1 | a0001c0002t0003g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.908+283A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/17 | chr13 | 31150664 | |||||||
| chr13:31150758 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.908+189A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 7/17 | chr13 | 31150758 | |||||||
| chr13:31151237 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.664-46A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151237 | |||||||
| chr13:31151276 | A | C | 1 | a0001c0001t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.664-85T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151276 | |||||||
| chr13:31151402 | T | C | 2 | a0001c0001t0004g0127 a0001c0001t0004g0128 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.663+207A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151402 | |||||||
| chr13:31151435 | G | C | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663+174C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151435 | |||||||
| chr13:31151480 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.663+129G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151480 | |||||||
| chr13:31151517 | C | T | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663+92G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151517 | |||||||
| chr13:31151595 | A | C | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.663+14T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 6/17 | chr13 | 31151595 | |||||||
| chr13:31151805 | A | C | 1 | a0001c0001t0004g0113 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.530-63T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31151805 | |||||||
| chr13:31151975 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0180 |
3 | HG01074.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.530-233C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31151975 | |||||||
| chr13:31151990 | G | A | 2 | a0001c0001t0005g0019 a0001c0001t0005g0116 |
4 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-248C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31151990 | |||||||
| chr13:31152022 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0087 others(7): Show |
22 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.530-280C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152022 | |||||||
| chr13:31152041 | T | C | 30 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(27): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.530-299A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152041 | |||||||
| chr13:31152333 | C | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0128 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+519G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152333 | |||||||
| chr13:31152345 | T | C | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.529+507A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152345 | |||||||
| chr13:31152420 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
170 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.529+432A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152420 | |||||||
| chr13:31152491 | T | A | 1 | a0001c0001t0002g0044 | 2 | NA19001.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.529+361A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152491 | |||||||
| chr13:31152516 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
170 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.529+336A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152516 | |||||||
| chr13:31152571 | C | G | 1 | a0001c0001t0002g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.529+281G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152571 | |||||||
| chr13:31152592 | G | A | 5 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+260C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 5/17 | chr13 | 31152592 | |||||||
| chr13:31153010 | T | A | 5 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-59A>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153010 | |||||||
| chr13:31153023 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.430-72T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153023 | |||||||
| chr13:31153114 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.430-163C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153114 | |||||||
| chr13:31153137 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
3 | NA18955.hp1 NA18975.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.430-186C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153137 | |||||||
| chr13:31153153 | C | T | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.430-202G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153153 | |||||||
| chr13:31153172 | C | G | 1 | a0001c0001t0005g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.430-221G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153172 | |||||||
| chr13:31153217 | A | C | 1 | a0001c0001t0005g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.430-266T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153217 | |||||||
| chr13:31153363 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.430-412T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153363 | |||||||
| chr13:31153377 | C | T | 1 | a0001c0007t0001g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.430-426G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153377 | |||||||
| chr13:31153722 | T | C | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-771A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153722 | |||||||
| chr13:31153835 | C | CA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
159 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.429+797dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153835 | |||||||
| chr13:31153835 | C | CAA | 28 | a0001c0001t0001g0092 a0001c0002t0003g0004 a0001c0002t0003g0010 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.429+796_429+797dup others(2): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153835 | |||||||
| chr13:31153835 | CA | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+797delT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31153835 | |||||||
| chr13:31154025 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
170 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.429+608T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154025 | |||||||
| chr13:31154119 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.429+514G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154119 | |||||||
| chr13:31154212 | G | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.429+421C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154212 | |||||||
| chr13:31154254 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.429+379G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154254 | |||||||
| chr13:31154255 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.429+378C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154255 | |||||||
| chr13:31154271 | T | C | 1 | a0001c0001t0005g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.429+362A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154271 | |||||||
| chr13:31154291 | G | A | 7 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(4): Show |
11 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+342C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154291 | |||||||
| chr13:31154417 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG02155.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.429+216G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154417 | |||||||
| chr13:31154502 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.429+131G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154502 | |||||||
| chr13:31154520 | T | C | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.429+113A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154520 | |||||||
| chr13:31154529 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.429+104C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154529 | |||||||
| chr13:31154560 | A | T | 1 | a0001c0001t0008g0190 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+73T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154560 | |||||||
| chr13:31154566 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.429+67A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154566 | |||||||
| chr13:31154626 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02080.hp2 | splice_region_variant&intron_variant | LOW | c.429+7A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 4/17 | chr13 | 31154626 | |||||||
| chr13:31154871 | T | C | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.307-116A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31154871 | |||||||
| chr13:31154886 | G | A | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-131C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31154886 | |||||||
| chr13:31154943 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 |
10 | HG00609.hp1 NA18747.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-188T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31154943 | |||||||
| chr13:31155002 | A | C | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.307-247T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31155002 | |||||||
| chr13:31155299 | A | T | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+215T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31155299 | |||||||
| chr13:31155337 | T | G | 2 | a0001c0001t0005g0019 a0001c0001t0005g0116 |
4 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+177A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31155337 | |||||||
| chr13:31155391 | G | A | 1 | a0001c0002t0003g0041 | 2 | HG03927.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+123C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31155391 | |||||||
| chr13:31155469 | G | A | 1 | a0001c0002t0003g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.306+45C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 3/17 | chr13 | 31155469 | |||||||
| chr13:31155752 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.166-98T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31155752 | |||||||
| chr13:31155994 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0100 |
3 | HG02055.hp2 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.166-340G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31155994 | |||||||
| chr13:31156117 | G | A | 7 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0094 others(4): Show |
11 | HG01106.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-463C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156117 | |||||||
| chr13:31156194 | T | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-540A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156194 | |||||||
| chr13:31156222 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.166-568G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156222 | |||||||
| chr13:31156394 | C | CA | 29 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0041 others(26): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.166-741dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156394 | |||||||
| chr13:31156420 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.166-766A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156420 | |||||||
| chr13:31156464 | T | C | 1 | a0001c0001t0006g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.166-810A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156464 | |||||||
| chr13:31156469 | C | T | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-815G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156469 | |||||||
| chr13:31156472 | G | C | 4 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(1): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-818C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156472 | |||||||
| chr13:31156564 | C | CA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.166-911dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156564 | |||||||
| chr13:31156835 | C | T | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1181G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156835 | |||||||
| chr13:31156865 | G | C | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-1211C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156865 | |||||||
| chr13:31156889 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.166-1235C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156889 | |||||||
| chr13:31156911 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
168 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.166-1257A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156911 | |||||||
| chr13:31156940 | T | C | 1 | a0001c0001t0004g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.166-1286A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156940 | |||||||
| chr13:31156991 | A | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.166-1337T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31156991 | |||||||
| chr13:31157116 | T | C | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-1462A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157116 | |||||||
| chr13:31157195 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
168 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.166-1541C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157195 | |||||||
| chr13:31157197 | C | T | 1 | a0001c0001t0006g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.166-1543G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157197 | |||||||
| chr13:31157279 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.165+1527A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157279 | |||||||
| chr13:31157459 | T | C | 1 | a0001c0002t0003g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.165+1347A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157459 | |||||||
| chr13:31157532 | T | G | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.165+1274A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157532 | |||||||
| chr13:31157769 | T | C | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.165+1037A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157769 | |||||||
| chr13:31157778 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+1028A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157778 | |||||||
| chr13:31157875 | G | T | 2 | a0001c0001t0004g0112 a0001c0001t0011g0037 |
3 | NA18941.hp2 NA18974.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.165+931C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157875 | |||||||
| chr13:31157928 | TTTAC | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.165+874_165+877del others(4): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31157928 | |||||||
| chr13:31158122 | C | G | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.165+684G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158122 | |||||||
| chr13:31158242 | CAAAAAGT others(11): Show |
C | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.165+546_165+563del others(18): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158242 | |||||||
| chr13:31158311 | G | A | 4 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0127 others(1): Show |
4 | HG02615.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+495C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158311 | |||||||
| chr13:31158347 | G | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.165+459C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158347 | |||||||
| chr13:31158413 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.165+393C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158413 | |||||||
| chr13:31158422 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.165+384C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158422 | |||||||
| chr13:31158443 | G | A | 1 | a0001c0001t0001g0009 | 5 | HG02523.hp2 NA18957.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+363C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158443 | |||||||
| chr13:31158454 | C | T | 1 | a0001c0001t0012g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.165+352G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158454 | |||||||
| chr13:31158481 | G | A | 5 | a0001c0001t0008g0026 a0001c0001t0008g0190 a0001c0001t0008g0191 others(2): Show |
7 | HG02280.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+325C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158481 | |||||||
| chr13:31158548 | C | CA | 20 | a0001c0001t0002g0045 a0001c0001t0002g0173 a0001c0001t0002g0174 others(17): Show |
43 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.165+257dupT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158548 | |||||||
| chr13:31158548 | CA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
164 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(161): Show |
intron_variant | MODIFIER | c.165+257delT | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158548 | |||||||
| chr13:31158548 | CAA | C | 22 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0002t0003g0004 others(19): Show |
46 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.165+256_165+257del others(2): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158548 | |||||||
| chr13:31158574 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.165+232C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158574 | |||||||
| chr13:31158592 | G | A | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+214C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158592 | |||||||
| chr13:31158605 | G | A | 1 | a0001c0002t0003g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.165+201C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158605 | |||||||
| chr13:31158682 | T | C | 1 | a0001c0001t0005g0117 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165+124A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158682 | |||||||
| chr13:31158724 | T | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.165+82A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158724 | |||||||
| chr13:31158730 | C | T | 1 | a0001c0001t0002g0043 | 2 | HG01123.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.165+76G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 2/17 | chr13 | 31158730 | |||||||
| chr13:31158920 | G | A | 14 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0046 others(11): Show |
27 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-57C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31158920 | |||||||
| chr13:31158921 | A | G | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-58T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31158921 | |||||||
| chr13:31159058 | G | A | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.108-195C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159058 | |||||||
| chr13:31159092 | G | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.108-229C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159092 | |||||||
| chr13:31159115 | CCA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.108-254_108-253del others(2): Show |
HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159115 | |||||||
| chr13:31159189 | A | G | 1 | a0001c0001t0004g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.108-326T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159189 | |||||||
| chr13:31159211 | T | C | 30 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(27): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.108-348A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159211 | |||||||
| chr13:31159215 | A | G | 1 | a0001c0001t0002g0042 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.108-352T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159215 | |||||||
| chr13:31159307 | A | C | 2 | a0001c0001t0016g0104 a0001c0001t0017g0105 |
2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.108-444T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159307 | |||||||
| chr13:31159307 | A | G | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-444T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159307 | |||||||
| chr13:31159341 | A | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-478T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159341 | |||||||
| chr13:31159364 | G | A | 3 | a0001c0001t0005g0021 a0001c0001t0005g0118 a0001c0001t0005g0119 |
5 | HG00423.hp2 NA18986.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-501C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159364 | |||||||
| chr13:31159458 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.108-595C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159458 | |||||||
| chr13:31159607 | G | A | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.108-744C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159607 | |||||||
| chr13:31159613 | T | G | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-750A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159613 | |||||||
| chr13:31159719 | A | T | 1 | a0001c0002t0003g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.108-856T>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159719 | |||||||
| chr13:31159750 | G | T | 5 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-887C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159750 | |||||||
| chr13:31159759 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.108-896C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159759 | |||||||
| chr13:31159808 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.108-945A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159808 | |||||||
| chr13:31159852 | G | A | 1 | a0001c0002t0003g0155 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.108-989C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159852 | |||||||
| chr13:31159864 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108-1001T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159864 | |||||||
| chr13:31159866 | C | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0128 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.108-1003G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159866 | |||||||
| chr13:31159875 | G | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.108-1012C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159875 | |||||||
| chr13:31159915 | G | A | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-1052C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159915 | |||||||
| chr13:31159976 | G | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(30): Show |
86 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.108-1113C>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159976 | |||||||
| chr13:31159999 | G | A | 1 | a0001c0002t0003g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.108-1136C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159999 | |||||||
| chr13:31159999 | G | C | 27 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(24): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.108-1136C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31159999 | |||||||
| chr13:31160272 | C | T | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.107+1204G>A | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160272 | |||||||
| chr13:31160552 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.107+924C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160552 | |||||||
| chr13:31160630 | C | A | 1 | a0001c0001t0004g0121 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.107+846G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160630 | |||||||
| chr13:31160653 | A | C | 7 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+823T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160653 | |||||||
| chr13:31160679 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.107+797A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160679 | |||||||
| chr13:31160750 | A | G | 1 | a0002c0004t0010g0022 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.107+726T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160750 | |||||||
| chr13:31160809 | C | G | 1 | a0001c0010t0025g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+667G>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160809 | |||||||
| chr13:31160870 | G | A | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.107+606C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160870 | |||||||
| chr13:31160971 | T | G | 1 | a0001c0001t0002g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.107+505A>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31160971 | |||||||
| chr13:31161000 | C | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.107+476G>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161000 | |||||||
| chr13:31161005 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.107+471T>C | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161005 | |||||||
| chr13:31161049 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
157 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.107+427T>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161049 | |||||||
| chr13:31161130 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.107+346C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161130 | |||||||
| chr13:31161154 | G | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | NA18997.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.107+322C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161154 | |||||||
| chr13:31161244 | G | A | 1 | a0001c0001t0005g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.107+232C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161244 | |||||||
| chr13:31161263 | G | A | 28 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0040 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.107+213C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161263 | |||||||
| chr13:31161325 | G | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02040.hp1 NA18970.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.107+151C>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161325 | |||||||
| chr13:31161339 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.107+137A>G | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161339 | |||||||
| chr13:31161372 | G | A | 2 | a0001c0006t0014g0186 a0001c0006t0014g0187 |
2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.107+104C>T | HSPH1 | ENSG00000120694.20 | transcript | ENST00000320027.10 | protein_coding | 1/17 | chr13 | 31161372 |