Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7060 |
| ensemblid | ENSG00000113296.14 |
| hgncid | 11788 |
| symbol | THBS4 |
| name | thrombospondin 4 |
| refseq_nuc | NM_003248.6 |
| refseq_prot | NP_003239.2 |
| ensembl_nuc | ENST00000350881.6 |
| ensembl_prot | ENSP00000339730.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 80035348 |
| end | 80083287 |
| strand | + |
| ver | v1.2 |
| region | chr5:80035348-80083287 |
| region5000 | chr5:80030348-80088287 |
| regionname0 | THBS4_chr5_80035348_80083287 |
| regionname5000 | THBS4_chr5_80030348_80088287 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 961 | 317 | 57 | 44 | 166 | 13 | 35 | 123 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0002 | 0/0 | 961 | 57 | 10 | 16 | 23 | 2 | 6 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0003 | 0/0 | 961 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0004 | 0/0 | 961 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0005 | 0/0 | 961 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0006 | 0/0 | 961 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0007 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0008 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0009 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0010 | 0/0 | 961 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| a0011 | 0/0 | 961 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | MLAPR others(956): Show |
chr5 | 80030348 | 80088287 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2883 | 148 | 24 | 10 | 85 | 6 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0001c0002 | 0/0 | 2883 | 88 | 14 | 23 | 36 | 5 | 10 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0001c0003 | 0/0 | 2883 | 79 | 17 | 11 | 45 | 2 | 4 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0001c0010 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0002c0004 | 0/0 | 2883 | 38 | 10 | 16 | 5 | 2 | 5 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0002c0005 | 0/0 | 2883 | 11 | 0 | 0 | 11 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0002c0007 | 0/0 | 2883 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0002c0013 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0003c0006 | 0/0 | 2883 | 7 | 0 | 7 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0004c0008 | 0/0 | 2883 | 4 | 3 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0005c0009 | 0/0 | 2883 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0006c0012 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0007c0015 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0008c0011 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0009c0017 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0010c0016 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 | ||
| a0011c0014 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | ATGCT others(2878): Show |
chr5 | 80030348 | 80088287 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3222 | 145 | 24 | 10 | 84 | 5 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0001t0004 | 1/0 | 3222 | 2 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0001t0005 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0002t0001 | 0/0 | 3222 | 83 | 14 | 19 | 36 | 5 | 9 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0002t0003 | 0/0 | 3222 | 5 | 0 | 4 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0003t0001 | 0/0 | 3222 | 78 | 17 | 11 | 44 | 2 | 4 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0003t0006 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0001c0010t0001 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0002c0004t0001 | 0/0 | 3222 | 38 | 10 | 16 | 5 | 2 | 5 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0002c0005t0001 | 0/0 | 3222 | 11 | 0 | 0 | 11 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0002c0007t0002 | 0/0 | 3222 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0002c0013t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0003c0006t0001 | 0/0 | 3222 | 7 | 0 | 7 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0004c0008t0001 | 0/0 | 3222 | 4 | 3 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0005c0009t0001 | 0/0 | 3222 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0006c0012t0001 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0007c0015t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0008c0011t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0009c0017t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0010c0016t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| a0011c0014t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | AGCAG others(3217): Show |
chr5 | 80030348 | 80088287 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 7 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0005 | 0/1 | 4 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0004g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0002 | 0/0 | 10 | 0 | 7 | 0 | 1 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0003t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0010t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0001c0010t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0007t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0007t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0007t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0002c0013t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0003c0006t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0003c0006t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0003c0006t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0003c0006t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0004c0008t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0004c0008t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0005c0009t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0005c0009t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0005c0009t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0006c0012t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0007c0015t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0008c0011t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0009c0017t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0010c0016t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| a0011c0014t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0271 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0034 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0002 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00408 | hp1 | a0002 | c0005 | t0001 | g0194 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00408 | hp2 | a0006 | c0012 | t0001 | g0007 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0175 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00733 | hp1 | a0002 | c0004 | t0001 | g0244 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0220 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0243 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01069 | hp1 | a0002 | c0004 | t0001 | g0173 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0221 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0268 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01109 | hp2 | a0002 | c0004 | t0001 | g0030 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01167 | hp1 | a0002 | c0004 | t0001 | g0010 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01168 | hp2 | a0002 | c0004 | t0001 | g0312 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01169 | hp2 | a0002 | c0004 | t0001 | g0010 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0222 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01243 | hp2 | a0004 | c0008 | t0001 | g0014 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0276 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01258 | hp2 | a0003 | c0006 | t0001 | g0080 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0174 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0040 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01515 | hp1 | a0002 | c0004 | t0001 | g0030 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0251 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0250 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01884 | hp1 | a0007 | c0015 | t0001 | g0024 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0235 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01891 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01952 | hp2 | a0003 | c0006 | t0001 | g0020 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01975 | hp1 | a0003 | c0006 | t0001 | g0001 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01978 | hp2 | a0002 | c0004 | t0001 | g0219 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02004 | hp1 | a0003 | c0006 | t0001 | g0009 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0242 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0315 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02148 | hp1 | a0003 | c0006 | t0001 | g0020 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0041 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02257 | hp1 | a0005 | c0009 | t0001 | g0301 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02273 | hp1 | a0003 | c0006 | t0001 | g0009 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02280 | hp1 | a0002 | c0004 | t0001 | g0180 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02293 | hp1 | a0003 | c0006 | t0001 | g0009 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0034 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0178 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0267 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02683 | hp1 | a0002 | c0004 | t0001 | g0186 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0181 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02723 | hp1 | a0001 | c0010 | t0001 | g0245 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0227 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02896 | hp2 | a0008 | c0011 | t0001 | g0216 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02965 | hp1 | a0001 | c0010 | t0001 | g0246 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03041 | hp1 | a0004 | c0008 | t0001 | g0263 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03130 | hp2 | a0009 | c0017 | t0001 | g0256 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0308 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03239 | hp2 | a0002 | c0004 | t0001 | g0184 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0166 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0234 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0185 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0224 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03540 | hp1 | a0005 | c0009 | t0001 | g0280 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03579 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03688 | hp1 | a0002 | c0013 | t0001 | g0099 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0259 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03942 | hp1 | a0010 | c0016 | t0001 | g0177 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04199 | hp1 | a0002 | c0004 | t0001 | g0010 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18522 | hp2 | a0004 | c0008 | t0001 | g0014 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0172 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18940 | hp2 | a0002 | c0004 | t0001 | g0183 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0161 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18947 | hp2 | a0002 | c0007 | t0002 | g0029 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18948 | hp2 | a0002 | c0007 | t0002 | g0028 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18952 | hp1 | a0002 | c0007 | t0002 | g0159 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18954 | hp2 | a0002 | c0007 | t0002 | g0028 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18974 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18988 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18993 | hp1 | a0002 | c0007 | t0002 | g0029 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19002 | hp2 | a0002 | c0004 | t0001 | g0182 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19003 | hp1 | a0002 | c0005 | t0001 | g0208 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19006 | hp1 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0189 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19043 | hp2 | a0004 | c0008 | t0001 | g0014 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19054 | hp2 | a0002 | c0004 | t0001 | g0179 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19056 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19058 | hp2 | a0002 | c0007 | t0002 | g0160 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19060 | hp2 | a0001 | c0003 | t0006 | g0168 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19064 | hp2 | a0002 | c0004 | t0001 | g0195 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19065 | hp1 | a0002 | c0005 | t0001 | g0210 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19075 | hp1 | a0002 | c0005 | t0001 | g0209 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19077 | hp2 | a0002 | c0005 | t0001 | g0188 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19079 | hp1 | a0002 | c0005 | t0001 | g0211 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19081 | hp1 | a0002 | c0005 | t0001 | g0197 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19091 | hp2 | a0002 | c0007 | t0002 | g0158 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA19240 | hp2 | a0002 | c0004 | t0001 | g0196 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20129 | hp2 | a0002 | c0004 | t0001 | g0314 | AFR | ASW | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0225 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0270 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA20805 | hp2 | a0011 | c0014 | t0001 | g0142 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0176 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0317 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03471 | hp1 | a0005 | c0009 | t0001 | g0293 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0316 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | USA | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0237 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0005 | REF | REF | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0022 | REF | REF | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80055899 | G | A | 1 | a0008 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.407G>A | p.Arg136Gln | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 597/3222 | 407/2886 | 136/961 | chr5 | 80055899 | |||
| chr5:80058737 | A | G | 1 | a0009 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.679A>G | p.Met227Val | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/22 | 869/3222 | 679/2886 | 227/961 | chr5 | 80058737 | |||
| chr5:80059736 | C | T | 1 | a0005 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.818C>T | p.Thr273Met | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/22 | 1008/3222 | 818/2886 | 273/961 | chr5 | 80059736 | |||
| chr5:80061729 | G | A | 1 | a0006 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1022G>A | p.Cys341Tyr | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/22 | 1212/3222 | 1022/2886 | 341/961 | chr5 | 80061729 | |||
| chr5:80065442 | G | C | 3 | a0002 a0008 a0010 |
59 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(56): Show |
missense_variant | MODERATE | c.1159G>C | p.Ala387Pro | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/22 | 1349/3222 | 1159/2886 | 387/961 | chr5 | 80065442 | |||
| chr5:80070405 | A | C | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1447A>C | p.Lys483Gln | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 11/22 | 1637/3222 | 1447/2886 | 483/961 | chr5 | 80070405 | |||
| chr5:80076898 | G | A | 1 | a0004 | 4 | HG01243.hp2 HG03041.hp1 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.1936G>A | p.Val646Ile | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/22 | 2126/3222 | 1936/2886 | 646/961 | chr5 | 80076898 | |||
| chr5:80078171 | G | A | 1 | a0003 | 7 | HG01258.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
missense_variant | MODERATE | c.2209G>A | p.Val737Ile | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/22 | 2399/3222 | 2209/2886 | 737/961 | chr5 | 80078171 | |||
| chr5:80079215 | C | T | 1 | a0011 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2468C>T | p.Ala823Val | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/22 | 2658/3222 | 2468/2886 | 823/961 | chr5 | 80079215 | |||
| chr5:80080056 | G | A | 1 | a0010 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2663G>A | p.Arg888Lys | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/22 | 2853/3222 | 2663/2886 | 888/961 | chr5 | 80080056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80035615 | C | T | 1 | a0002c0005 | 11 | HG00408.hp1 NA18942.hp1 NA18974.hp1 others(8): Show |
synonymous_variant | LOW | c.78C>T | p.Ala26Ala | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 268/3222 | 78/2886 | 26/961 | chr5 | 80035615 | |||
| chr5:80055912 | C | T | 5 | a0001c0002 a0002c0007 a0004c0008 others(2): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
synonymous_variant | LOW | c.420C>T | p.Ser140Ser | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 610/3222 | 420/2886 | 140/961 | chr5 | 80055912 | |||
| chr5:80056029 | A | T | 11 | a0001c0002 a0001c0003 a0001c0010 others(8): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
synonymous_variant | LOW | c.537A>T | p.Pro179Pro | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 727/3222 | 537/2886 | 179/961 | chr5 | 80056029 | |||
| chr5:80065459 | G | A | 1 | a0001c0010 | 2 | HG02723.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.1176G>A | p.Ser392Ser | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/22 | 1366/3222 | 1176/2886 | 392/961 | chr5 | 80065459 | |||
| chr5:80068110 | G | A | 1 | a0005c0009 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.1332G>A | p.Gly444Gly | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/22 | 1522/3222 | 1332/2886 | 444/961 | chr5 | 80068110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80035371 | A | G | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0002t0001 others(17): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
5_prime_UTR_variant | MODIFIER | c.-167A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 167 | chr5 | 80035371 | ||||||
| chr5:80035406 | C | G | 1 | a0002c0007t0002 | 7 | NA18947.hp2 NA18948.hp2 NA18952.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-132C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 132 | chr5 | 80035406 | ||||||
| chr5:80035420 | G | C | 1 | a0001c0001t0005 | 1 | NA19080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 118 | chr5 | 80035420 | ||||||
| chr5:80035461 | A | G | 1 | a0001c0003t0006 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 77 | chr5 | 80035461 | ||||||
| chr5:80083266 | G | A | 1 | a0001c0002t0003 | 5 | HG00733.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*125G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 22/22 | 125 | chr5 | 80083266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80035714 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.88+89C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80035714 | |||||||
| chr5:80036039 | A | G | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+414A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036039 | |||||||
| chr5:80036196 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+571G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036196 | |||||||
| chr5:80036325 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88+700G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036325 | |||||||
| chr5:80036519 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.88+894A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036519 | |||||||
| chr5:80036544 | T | G | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+919T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036544 | |||||||
| chr5:80036554 | C | A | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+929C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036554 | |||||||
| chr5:80036644 | G | A | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+1019G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036644 | |||||||
| chr5:80036857 | A | T | 1 | a0002c0004t0001g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+1232A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036857 | |||||||
| chr5:80037050 | C | A | 2 | a0002c0004t0001g0040 a0002c0004t0001g0041 |
2 | HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.88+1425C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037050 | |||||||
| chr5:80037282 | G | T | 1 | a0001c0002t0001g0313 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.88+1657G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037282 | |||||||
| chr5:80037440 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+1815G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037440 | |||||||
| chr5:80037562 | T | C | 3 | a0001c0001t0001g0045 a0001c0003t0001g0043 a0001c0003t0001g0044 |
3 | HG02559.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88+1937T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037562 | |||||||
| chr5:80037592 | G | T | 193 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0001t0001g0247 others(190): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.88+1967G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037592 | |||||||
| chr5:80037664 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+2039T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037664 | |||||||
| chr5:80037890 | C | T | 1 | a0002c0004t0001g0312 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.89-2187C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037890 | |||||||
| chr5:80038104 | A | T | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.89-1973A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038104 | |||||||
| chr5:80038215 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.89-1862G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038215 | |||||||
| chr5:80038287 | A | G | 1 | a0001c0001t0001g0027 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.89-1790A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038287 | |||||||
| chr5:80038403 | T | C | 7 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(4): Show |
7 | HG01358.hp1 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-1674T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038403 | |||||||
| chr5:80038470 | G | A | 101 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(98): Show |
128 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.89-1607G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038470 | |||||||
| chr5:80038573 | T | C | 1 | a0001c0002t0001g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.89-1504T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038573 | |||||||
| chr5:80038765 | C | T | 82 | a0001c0001t0001g0247 a0001c0002t0001g0008 a0001c0002t0001g0015 others(79): Show |
93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.89-1312C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038765 | |||||||
| chr5:80038940 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
9 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-1137A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038940 | |||||||
| chr5:80038958 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.89-1119A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038958 | |||||||
| chr5:80039095 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.89-982G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039095 | |||||||
| chr5:80039149 | T | C | 106 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(103): Show |
134 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.89-928T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039149 | |||||||
| chr5:80039444 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-633A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039444 | |||||||
| chr5:80039530 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.89-547G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039530 | |||||||
| chr5:80039663 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.89-414G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039663 | |||||||
| chr5:80039883 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.89-194T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039883 | |||||||
| chr5:80040447 | CG | C | 106 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(103): Show |
132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.292+174delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80040447 | ||||||
| chr5:80040454 | G | T | 1 | a0001c0003t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292+174G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040454 | |||||||
| chr5:80040455 | T | G | 1 | a0001c0003t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292+175T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040455 | |||||||
| chr5:80040868 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.292+588A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040868 | |||||||
| chr5:80040888 | G | T | 1 | a0001c0003t0001g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.292+608G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040888 | |||||||
| chr5:80040933 | ACT | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
5 | HG03130.hp1 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+659_292+660del others(2): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80040933 | ||||||
| chr5:80041003 | G | A | 1 | a0001c0002t0001g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.292+723G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041003 | |||||||
| chr5:80041153 | C | T | 1 | a0001c0003t0001g0238 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.292+873C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041153 | |||||||
| chr5:80041162 | G | A | 1 | a0002c0005t0001g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.292+882G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041162 | |||||||
| chr5:80041203 | T | A | 1 | a0002c0004t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+923T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041203 | |||||||
| chr5:80041264 | T | C | 1 | a0001c0003t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.292+984T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041264 | |||||||
| chr5:80041334 | C | T | 108 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(105): Show |
134 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.292+1054C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041334 | |||||||
| chr5:80041408 | C | G | 3 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0003t0001g0237 |
3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.292+1128C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041408 | |||||||
| chr5:80041418 | C | T | 1 | a0001c0002t0001g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+1138C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041418 | |||||||
| chr5:80041484 | C | T | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+1204C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041484 | |||||||
| chr5:80041543 | G | A | 4 | a0001c0002t0001g0248 a0001c0002t0001g0249 a0001c0002t0001g0250 others(1): Show |
4 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+1263G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041543 | |||||||
| chr5:80041644 | G | T | 1 | a0001c0003t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+1364G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041644 | |||||||
| chr5:80041709 | T | A | 1 | a0001c0003t0001g0164 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.292+1429T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041709 | |||||||
| chr5:80041759 | T | A | 3 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 |
3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+1479T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041759 | |||||||
| chr5:80041772 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.292+1492T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041772 | |||||||
| chr5:80041880 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292+1600A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041880 | |||||||
| chr5:80041992 | T | C | 1 | a0001c0003t0001g0167 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.292+1712T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041992 | |||||||
| chr5:80042310 | C | T | 3 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0003t0001g0237 |
3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.292+2030C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042310 | |||||||
| chr5:80042438 | A | C | 2 | a0001c0003t0001g0232 a0001c0003t0001g0233 |
2 | NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.292+2158A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042438 | |||||||
| chr5:80042823 | A | G | 199 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0213 others(196): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.292+2543A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042823 | |||||||
| chr5:80042869 | G | A | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+2589G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042869 | |||||||
| chr5:80042913 | C | T | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+2633C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042913 | |||||||
| chr5:80042929 | G | A | 2 | a0001c0003t0001g0169 a0001c0003t0006g0168 |
2 | NA18973.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.292+2649G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042929 | |||||||
| chr5:80043224 | C | T | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+2944C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043224 | |||||||
| chr5:80043347 | G | A | 12 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(9): Show |
12 | HG00423.hp2 HG00597.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+3067G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043347 | |||||||
| chr5:80043614 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.292+3334G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043614 | |||||||
| chr5:80043997 | C | T | 3 | a0001c0002t0001g0249 a0001c0002t0001g0250 a0001c0002t0001g0251 |
3 | HG01515.hp2 HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.292+3717C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043997 | |||||||
| chr5:80044031 | G | C | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+3751G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044031 | |||||||
| chr5:80044128 | T | C | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+3848T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044128 | |||||||
| chr5:80044193 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18957.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.292+3913C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044193 | |||||||
| chr5:80044414 | TA | T | 91 | a0001c0001t0001g0150 a0001c0002t0001g0008 a0001c0002t0001g0015 others(88): Show |
102 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.292+4144delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044414 | ||||||
| chr5:80044416 | A | G | 1 | a0001c0003t0001g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.292+4136A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044416 | |||||||
| chr5:80044570 | G | A | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+4290G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044570 | |||||||
| chr5:80044644 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292+4364C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044644 | |||||||
| chr5:80044677 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+4397G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044677 | |||||||
| chr5:80044707 | G | C | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+4427G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044707 | |||||||
| chr5:80044730 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.292+4450A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044730 | |||||||
| chr5:80044733 | AT | A | 90 | a0001c0001t0001g0065 a0001c0002t0001g0008 a0001c0002t0001g0015 others(87): Show |
101 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.292+4464delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044733 | ||||||
| chr5:80044756 | A | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+4476A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044756 | |||||||
| chr5:80044886 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.292+4606T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044886 | |||||||
| chr5:80044942 | G | A | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+4662G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044942 | |||||||
| chr5:80044987 | ATCTCTGA others(3): Show |
A | 3 | a0001c0002t0001g0249 a0001c0002t0001g0250 a0001c0002t0001g0251 |
3 | HG01515.hp2 HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.292+4713_292+4722d others(12): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044987 | ||||||
| chr5:80045072 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.292+4792A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045072 | |||||||
| chr5:80045339 | A | C | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+5059A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045339 | |||||||
| chr5:80045399 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.292+5119G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045399 | |||||||
| chr5:80045531 | C | CT | 14 | a0001c0001t0001g0129 a0001c0002t0001g0307 a0001c0003t0001g0002 others(11): Show |
24 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+5267dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80045531 | ||||||
| chr5:80045531 | CT | C | 15 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0067 others(12): Show |
16 | HG00621.hp2 HG01070.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+5267delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80045531 | ||||||
| chr5:80045552 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0007c0015t0001g0024 |
3 | HG01884.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.292+5272C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045552 | |||||||
| chr5:80045592 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.292+5312G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045592 | |||||||
| chr5:80045640 | C | G | 4 | a0001c0002t0003g0220 a0002c0004t0001g0219 a0002c0004t0001g0221 others(1): Show |
4 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+5360C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045640 | |||||||
| chr5:80045671 | T | C | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+5391T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045671 | |||||||
| chr5:80045687 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.292+5407G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045687 | |||||||
| chr5:80045746 | A | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+5466A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045746 | |||||||
| chr5:80045797 | C | T | 1 | a0001c0002t0001g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.292+5517C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045797 | |||||||
| chr5:80045810 | C | T | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292+5530C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045810 | |||||||
| chr5:80046019 | C | T | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292+5739C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046019 | |||||||
| chr5:80046021 | A | T | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292+5741A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046021 | |||||||
| chr5:80046048 | A | G | 90 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+5768A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046048 | |||||||
| chr5:80046166 | C | A | 93 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(90): Show |
119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.292+5886C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046166 | |||||||
| chr5:80046197 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292+5917A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046197 | |||||||
| chr5:80046603 | T | C | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.292+6323T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046603 | |||||||
| chr5:80046695 | C | T | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292+6415C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046695 | |||||||
| chr5:80046696 | G | A | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+6416G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046696 | |||||||
| chr5:80046713 | A | G | 2 | a0001c0002t0001g0304 a0001c0002t0001g0305 |
2 | HG02071.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.292+6433A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046713 | |||||||
| chr5:80047550 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.292+7270G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047550 | |||||||
| chr5:80047632 | A | AAT | 11 | a0001c0003t0001g0002 a0001c0003t0001g0033 a0001c0003t0001g0169 others(8): Show |
21 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.292+7353_292+7354d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80047632 | ||||||
| chr5:80047634 | T | TA | 97 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(94): Show |
115 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.292+7354_292+7355i others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047634 | |||||||
| chr5:80047635 | T | A | 5 | a0001c0003t0001g0187 a0001c0003t0006g0168 a0002c0004t0001g0312 others(2): Show |
5 | HG01168.hp2 NA18942.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+7355T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047635 | |||||||
| chr5:80047636 | T | A | 21 | a0001c0002t0003g0220 a0002c0004t0001g0010 a0002c0004t0001g0030 others(18): Show |
24 | HG00642.hp1 HG00733.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+7356T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047636 | |||||||
| chr5:80047692 | G | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0038 others(10): Show |
15 | HG01361.hp1 HG02698.hp1 HG03491.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+7412G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047692 | |||||||
| chr5:80047977 | C | T | 1 | a0001c0003t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292+7697C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047977 | |||||||
| chr5:80047979 | C | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+7699C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047979 | |||||||
| chr5:80048306 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-7479C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048306 | |||||||
| chr5:80048466 | T | C | 104 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0003g0220 others(101): Show |
130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.293-7319T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048466 | |||||||
| chr5:80048632 | A | ATG | 12 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0079 others(9): Show |
14 | HG01258.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-7121_293-7120d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | A | ATGTG | 58 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0001t0001g0078 others(55): Show |
75 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.293-7123_293-7120d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | A | ATGTGTG | 53 | a0001c0002t0001g0253 a0001c0002t0001g0266 a0001c0002t0001g0269 others(50): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.293-7125_293-7120d others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | A | ATGTGTGT others(1): Show |
36 | a0001c0002t0001g0036 a0001c0002t0001g0248 a0001c0002t0001g0259 others(33): Show |
41 | HG00408.hp1 HG00597.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.293-7127_293-7120d others(10): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | A | ATGTGTGT others(3): Show |
17 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-7129_293-7120d others(12): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | A | ATGTGTGT others(5): Show |
12 | a0001c0002t0001g0035 a0001c0002t0001g0249 a0001c0002t0001g0252 others(9): Show |
15 | HG01069.hp1 HG02071.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.293-7131_293-7120d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | ATG | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0046 others(9): Show |
15 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-7121_293-7120d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | ATGTG | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
8 | HG01123.hp2 HG02027.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-7123_293-7120d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048632 | ATGTGTGT others(5): Show |
A | 5 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0001c0010t0001g0245 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-7131_293-7120d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | ||||||
| chr5:80048795 | T | C | 47 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(44): Show |
65 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.293-6990T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048795 | |||||||
| chr5:80048837 | T | C | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-6948T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048837 | |||||||
| chr5:80049098 | C | T | 1 | a0002c0004t0001g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.293-6687C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049098 | |||||||
| chr5:80049145 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.293-6640A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049145 | |||||||
| chr5:80049314 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-6471G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049314 | |||||||
| chr5:80049387 | A | G | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.293-6398A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049387 | |||||||
| chr5:80049726 | G | T | 103 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0003t0001g0002 others(100): Show |
129 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.293-6059G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049726 | |||||||
| chr5:80049846 | A | G | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-5939A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049846 | |||||||
| chr5:80049978 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293-5807C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049978 | |||||||
| chr5:80049982 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.293-5803C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049982 | |||||||
| chr5:80049987 | A | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-5798A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049987 | |||||||
| chr5:80050194 | A | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02027.hp1 HG02129.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-5591A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050194 | |||||||
| chr5:80050361 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.293-5424T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050361 | |||||||
| chr5:80050519 | A | C | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-5266A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050519 | |||||||
| chr5:80050592 | G | C | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-5193G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050592 | |||||||
| chr5:80050620 | T | G | 1 | a0001c0003t0001g0217 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.293-5165T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050620 | |||||||
| chr5:80050744 | G | C | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-5041G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050744 | |||||||
| chr5:80050776 | G | A | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.293-5009G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050776 | |||||||
| chr5:80050809 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-4976A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050809 | |||||||
| chr5:80050984 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-4801A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050984 | |||||||
| chr5:80051057 | C | T | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4728C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051057 | |||||||
| chr5:80051215 | A | G | 1 | a0001c0003t0001g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.293-4570A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051215 | |||||||
| chr5:80051304 | C | T | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-4481C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051304 | |||||||
| chr5:80051330 | TAATAA | T | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4449_293-4445d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80051330 | ||||||
| chr5:80051342 | T | C | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4443T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051342 | |||||||
| chr5:80051382 | A | C | 4 | a0001c0002t0001g0248 a0001c0002t0001g0249 a0001c0002t0001g0250 others(1): Show |
4 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-4403A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051382 | |||||||
| chr5:80051425 | T | C | 15 | a0001c0002t0001g0035 a0001c0002t0001g0241 a0001c0002t0001g0248 others(12): Show |
18 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-4360T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051425 | |||||||
| chr5:80051466 | G | A | 10 | a0001c0002t0001g0035 a0001c0002t0001g0241 a0001c0002t0001g0248 others(7): Show |
11 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-4319G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051466 | |||||||
| chr5:80051513 | C | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4272C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051513 | |||||||
| chr5:80051697 | C | T | 2 | a0001c0002t0001g0299 a0001c0002t0001g0300 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.293-4088C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051697 | |||||||
| chr5:80051703 | A | G | 1 | a0001c0002t0001g0258 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.293-4082A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051703 | |||||||
| chr5:80051816 | G | C | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3969G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051816 | |||||||
| chr5:80051934 | G | A | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3851G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051934 | |||||||
| chr5:80052606 | G | A | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3179G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052606 | |||||||
| chr5:80052616 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0003t0001g0043 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-3169A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052616 | |||||||
| chr5:80052673 | C | T | 5 | a0002c0007t0002g0028 a0002c0007t0002g0029 a0002c0007t0002g0158 others(2): Show |
7 | NA18947.hp2 NA18948.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-3112C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052673 | |||||||
| chr5:80052839 | T | A | 2 | a0002c0004t0001g0013 a0008c0011t0001g0216 |
4 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2946T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052839 | |||||||
| chr5:80052936 | G | A | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-2849G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052936 | |||||||
| chr5:80053206 | T | A | 1 | a0001c0002t0001g0305 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.293-2579T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053206 | |||||||
| chr5:80053334 | T | C | 11 | a0001c0003t0001g0002 a0001c0003t0001g0033 a0001c0003t0001g0169 others(8): Show |
21 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.293-2451T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053334 | |||||||
| chr5:80053406 | C | CT | 6 | a0001c0001t0001g0061 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG00558.hp2 HG01981.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2365dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | ||||||
| chr5:80053406 | CT | C | 200 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0120 others(197): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.293-2365delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | ||||||
| chr5:80053406 | CTT | C | 4 | a0001c0002t0001g0266 a0001c0002t0001g0278 a0002c0004t0001g0013 others(1): Show |
6 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2366_293-2365d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | ||||||
| chr5:80053582 | C | G | 198 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0002t0001g0008 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-2203C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053582 | |||||||
| chr5:80053590 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-2195C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053590 | |||||||
| chr5:80053611 | TG | T | 44 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0003t0001g0043 others(41): Show |
52 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.293-2172delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053611 | ||||||
| chr5:80053766 | T | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-2019T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053766 | |||||||
| chr5:80053781 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-2004G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053781 | |||||||
| chr5:80053955 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-1830G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053955 | |||||||
| chr5:80054134 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.293-1651C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054134 | |||||||
| chr5:80054156 | TTTC | T | 101 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(98): Show |
125 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.293-1626_293-1624d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054156 | ||||||
| chr5:80054157 | TTC | T | 5 | a0002c0004t0001g0013 a0002c0004t0001g0174 a0002c0004t0001g0315 others(2): Show |
7 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-1626_293-1625d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054157 | ||||||
| chr5:80054159 | C | CT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(1): Show |
7 | HG03130.hp1 HG03139.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-1611dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054159 | ||||||
| chr5:80054159 | C | CTT | 85 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(82): Show |
98 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.293-1612_293-1611d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054159 | ||||||
| chr5:80054164 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-1621T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054164 | |||||||
| chr5:80054176 | A | T | 3 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 |
3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.293-1609A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054176 | |||||||
| chr5:80054185 | C | T | 1 | a0001c0003t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-1600C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054185 | |||||||
| chr5:80054217 | C | T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.293-1568C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054217 | |||||||
| chr5:80054262 | C | T | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-1523C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054262 | |||||||
| chr5:80054318 | C | CT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0076 a0001c0001t0001g0109 others(2): Show |
6 | HG01361.hp1 HG02698.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-1447dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | ||||||
| chr5:80054318 | CTTTT | C | 106 | a0001c0002t0001g0253 a0001c0002t0001g0265 a0001c0003t0001g0002 others(103): Show |
132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.293-1450_293-1447d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | ||||||
| chr5:80054318 | CTTTTT | C | 89 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(86): Show |
102 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.293-1451_293-1447d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | ||||||
| chr5:80054342 | A | T | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.293-1443A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054342 | |||||||
| chr5:80054373 | T | A | 2 | a0001c0003t0001g0171 a0001c0003t0001g0172 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293-1412T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054373 | |||||||
| chr5:80054462 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-1323G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054462 | |||||||
| chr5:80054556 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.293-1229T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054556 | |||||||
| chr5:80054610 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-1175C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054610 | |||||||
| chr5:80054661 | C | T | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-1124C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054661 | |||||||
| chr5:80054903 | T | C | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-882T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054903 | |||||||
| chr5:80054944 | C | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-841C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054944 | |||||||
| chr5:80055041 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293-744G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055041 | |||||||
| chr5:80055101 | C | T | 3 | a0001c0003t0001g0171 a0001c0003t0001g0172 a0001c0003t0001g0239 |
3 | HG02258.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293-684C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055101 | |||||||
| chr5:80055112 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02027.hp1 HG02129.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-673G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055112 | |||||||
| chr5:80055131 | G | A | 2 | a0002c0004t0001g0040 a0002c0004t0001g0041 |
2 | HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.293-654G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055131 | |||||||
| chr5:80055227 | C | T | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(274): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.293-558C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055227 | |||||||
| chr5:80055264 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.293-521G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055264 | |||||||
| chr5:80055311 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-474G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055311 | |||||||
| chr5:80055317 | G | T | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-468G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055317 | |||||||
| chr5:80055588 | T | C | 195 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(192): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.293-197T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055588 | |||||||
| chr5:80055593 | GA | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-188delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80055593 | ||||||
| chr5:80055721 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-64G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055721 | |||||||
| chr5:80055721 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-64G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055721 | |||||||
| chr5:80056036 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.540+4G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056036 | |||||||
| chr5:80056037 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.540+5G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056037 | |||||||
| chr5:80056058 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+26A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056058 | |||||||
| chr5:80056125 | G | A | 3 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 |
3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.540+93G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056125 | |||||||
| chr5:80056354 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.540+322G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056354 | |||||||
| chr5:80056397 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540+365A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056397 | |||||||
| chr5:80056678 | GAACTAGT others(80): Show |
G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+652_540+738del others(87): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 80056678 | ||||||
| chr5:80056787 | T | C | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.540+755T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056787 | |||||||
| chr5:80056789 | C | T | 2 | a0001c0003t0001g0232 a0001c0003t0001g0233 |
2 | NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.540+757C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056789 | |||||||
| chr5:80056904 | T | C | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+872T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056904 | |||||||
| chr5:80057044 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.540+1012G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057044 | |||||||
| chr5:80057120 | A | T | 3 | a0001c0002t0001g0036 a0001c0002t0001g0297 a0001c0002t0001g0306 |
4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1086A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057120 | |||||||
| chr5:80057163 | G | A | 100 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(97): Show |
126 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.541-1043G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057163 | |||||||
| chr5:80057262 | C | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-944C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057262 | |||||||
| chr5:80057294 | T | G | 1 | a0001c0001t0001g0027 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.541-912T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057294 | |||||||
| chr5:80057605 | T | C | 8 | a0001c0003t0001g0002 a0001c0003t0001g0033 a0001c0003t0001g0223 others(5): Show |
18 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-601T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057605 | |||||||
| chr5:80057676 | C | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-530C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057676 | |||||||
| chr5:80057713 | G | A | 1 | a0002c0004t0001g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.541-493G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057713 | |||||||
| chr5:80057718 | A | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-488A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057718 | |||||||
| chr5:80057731 | G | A | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-475G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057731 | |||||||
| chr5:80057805 | A | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-401A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057805 | |||||||
| chr5:80057824 | C | T | 195 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(192): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.541-382C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057824 | |||||||
| chr5:80057895 | C | T | 1 | a0001c0003t0001g0193 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.541-311C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057895 | |||||||
| chr5:80058012 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541-194A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058012 | |||||||
| chr5:80058137 | G | A | 1 | a0001c0003t0001g0198 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.541-69G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058137 | |||||||
| chr5:80058143 | A | G | 1 | a0001c0002t0001g0037 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.541-63A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058143 | |||||||
| chr5:80058179 | C | A | 1 | a0005c0009t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.541-27C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058179 | |||||||
| chr5:80058324 | C | T | 197 | a0001c0001t0001g0081 a0001c0002t0001g0008 a0001c0002t0001g0015 others(194): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.649+10C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058324 | |||||||
| chr5:80058361 | A | G | 108 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(105): Show |
136 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.649+47A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058361 | |||||||
| chr5:80058363 | A | G | 1 | a0001c0003t0001g0238 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.649+49A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058363 | |||||||
| chr5:80058391 | C | G | 1 | a0001c0002t0001g0296 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.649+77C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058391 | |||||||
| chr5:80058398 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649+84T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058398 | |||||||
| chr5:80058470 | A | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.649+156A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058470 | |||||||
| chr5:80058544 | A | AT | 104 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(101): Show |
132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.650-156dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 80058544 | ||||||
| chr5:80058582 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.650-126A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058582 | |||||||
| chr5:80058824 | C | G | 196 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.732+34C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058824 | |||||||
| chr5:80058879 | C | T | 194 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(191): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.732+89C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058879 | |||||||
| chr5:80058905 | C | T | 85 | a0001c0001t0001g0075 a0001c0002t0001g0008 a0001c0002t0001g0015 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.732+115C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058905 | |||||||
| chr5:80058972 | GTGA | G | 3 | a0001c0002t0001g0036 a0001c0002t0001g0297 a0001c0002t0001g0306 |
4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+186_732+188del others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80058972 | ||||||
| chr5:80059025 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+235C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059025 | |||||||
| chr5:80059069 | T | C | 195 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(192): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.732+279T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059069 | |||||||
| chr5:80059172 | A | G | 3 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 |
3 | HG00642.hp2 HG01167.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.733-268A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059172 | |||||||
| chr5:80059199 | G | A | 195 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(192): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.733-241G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059199 | |||||||
| chr5:80059315 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.733-125C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059315 | |||||||
| chr5:80059327 | C | CA | 5 | a0001c0001t0001g0098 a0001c0001t0001g0122 a0001c0001t0001g0145 others(2): Show |
7 | HG00280.hp2 HG02027.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-94dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80059327 | ||||||
| chr5:80059327 | CA | C | 107 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0096 others(104): Show |
133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.733-94delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80059327 | ||||||
| chr5:80059341 | A | G | 1 | a0004c0008t0001g0014 | 3 | HG01243.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.733-99A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059341 | |||||||
| chr5:80059369 | T | A | 197 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(194): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.733-71T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059369 | |||||||
| chr5:80059555 | G | A | 1 | a0002c0004t0001g0221 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.784+64G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059555 | |||||||
| chr5:80059572 | C | T | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784+81C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059572 | |||||||
| chr5:80059648 | C | T | 89 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(86): Show |
100 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.785-55C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059648 | |||||||
| chr5:80059667 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.785-36C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059667 | |||||||
| chr5:80060001 | T | G | 1 | a0001c0002t0003g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.987+96T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060001 | |||||||
| chr5:80060106 | T | C | 3 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 |
3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.987+201T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060106 | |||||||
| chr5:80060169 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.987+264C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060169 | |||||||
| chr5:80060337 | C | T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.987+432C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060337 | |||||||
| chr5:80060424 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.987+519A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060424 | |||||||
| chr5:80060543 | T | G | 1 | a0002c0004t0001g0173 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.987+638T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060543 | |||||||
| chr5:80060759 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.987+854A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060759 | |||||||
| chr5:80060762 | CA | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0048 others(2): Show |
6 | HG03130.hp1 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+866delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 80060762 | ||||||
| chr5:80060808 | T | C | 1 | a0001c0003t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.988-887T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060808 | |||||||
| chr5:80060997 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.988-698G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060997 | |||||||
| chr5:80061039 | T | C | 1 | a0001c0002t0001g0311 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.988-656T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061039 | |||||||
| chr5:80061294 | G | A | 8 | a0002c0005t0001g0012 a0002c0005t0001g0161 a0002c0005t0001g0188 others(5): Show |
10 | HG00408.hp1 NA18942.hp1 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-401G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061294 | |||||||
| chr5:80061323 | C | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02027.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-372C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061323 | |||||||
| chr5:80061350 | C | T | 1 | a0001c0002t0001g0304 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.988-345C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061350 | |||||||
| chr5:80061361 | T | C | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.988-334T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061361 | |||||||
| chr5:80061515 | C | G | 1 | a0002c0004t0001g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.988-180C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061515 | |||||||
| chr5:80061613 | A | C | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.988-82A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061613 | |||||||
| chr5:80062045 | A | C | 1 | a0001c0003t0001g0206 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1125+213A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062045 | |||||||
| chr5:80062150 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+318T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062150 | |||||||
| chr5:80062491 | A | C | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+659A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062491 | |||||||
| chr5:80062495 | T | C | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+663T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062495 | |||||||
| chr5:80062496 | T | A | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+664T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062496 | |||||||
| chr5:80062498 | C | A | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+666C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062498 | |||||||
| chr5:80062499 | C | G | 37 | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0031 others(34): Show |
45 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1125+667C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062499 | |||||||
| chr5:80062503 | C | A | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+671C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062503 | |||||||
| chr5:80062506 | C | T | 1 | a0002c0004t0001g0183 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+674C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062506 | |||||||
| chr5:80062610 | G | A | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1125+778G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062610 | |||||||
| chr5:80062798 | C | T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1125+966C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062798 | |||||||
| chr5:80062804 | G | A | 3 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0003t0001g0237 |
3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1125+972G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062804 | |||||||
| chr5:80062837 | A | G | 1 | a0001c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1125+1005A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062837 | |||||||
| chr5:80062837 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1125+1005A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062837 | |||||||
| chr5:80063046 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1125+1214G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063046 | |||||||
| chr5:80063403 | T | TTAAG | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+1573_1125+157 others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 80063403 | ||||||
| chr5:80063419 | G | A | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+1587G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063419 | |||||||
| chr5:80063504 | G | T | 1 | a0002c0004t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1125+1672G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063504 | |||||||
| chr5:80063665 | A | G | 8 | a0001c0002t0001g0036 a0001c0002t0001g0257 a0001c0002t0001g0258 others(5): Show |
11 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1126-1744A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063665 | |||||||
| chr5:80063782 | G | C | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1126-1627G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063782 | |||||||
| chr5:80064215 | A | G | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1126-1194A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064215 | |||||||
| chr5:80064351 | T | C | 196 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(193): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1126-1058T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064351 | |||||||
| chr5:80064352 | G | A | 9 | a0001c0003t0001g0002 a0001c0003t0001g0033 a0001c0003t0001g0223 others(6): Show |
19 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1126-1057G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064352 | |||||||
| chr5:80064568 | T | C | 1 | a0001c0002t0001g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1126-841T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064568 | |||||||
| chr5:80064588 | G | A | 2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1126-821G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064588 | |||||||
| chr5:80064635 | G | T | 2 | a0001c0003t0001g0167 a0001c0003t0001g0192 |
2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1126-774G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064635 | |||||||
| chr5:80064688 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0131 |
2 | HG02698.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1126-721T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064688 | |||||||
| chr5:80064712 | A | T | 44 | a0002c0004t0001g0010 a0002c0004t0001g0013 a0002c0004t0001g0030 others(41): Show |
52 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1126-697A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064712 | |||||||
| chr5:80065003 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1126-406T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80065003 | |||||||
| chr5:80065059 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1126-350T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80065059 | |||||||
| chr5:80065579 | CATAAT | C | 84 | a0001c0001t0001g0132 a0001c0002t0001g0008 a0001c0002t0001g0015 others(81): Show |
95 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1194+106_1194+110d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80065579 | ||||||
| chr5:80065589 | T | A | 1 | a0011c0014t0001g0142 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1194+112T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80065589 | |||||||
| chr5:80065665 | T | C | 17 | a0001c0003t0001g0169 a0001c0003t0006g0168 a0002c0004t0001g0195 others(14): Show |
21 | HG00408.hp1 NA18942.hp1 NA18947.hp2 others(18): Show |
intron_variant | MODIFIER | c.1194+188T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80065665 | |||||||
| chr5:80066019 | C | T | 2 | a0001c0001t0001g0132 a0001c0002t0001g0309 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1194+542C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066019 | |||||||
| chr5:80066027 | G | A | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1194+550G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066027 | |||||||
| chr5:80066031 | C | T | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1194+554C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066031 | |||||||
| chr5:80066050 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+573G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066050 | |||||||
| chr5:80066093 | T | C | 7 | a0001c0002t0001g0036 a0001c0002t0001g0257 a0001c0002t0001g0258 others(4): Show |
10 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+616T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066093 | |||||||
| chr5:80066094 | C | CA | 17 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0047 others(14): Show |
19 | HG01261.hp2 HG01891.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1194+638dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | ||||||
| chr5:80066094 | C | CAA | 9 | a0001c0002t0001g0253 a0001c0002t0001g0264 a0001c0002t0001g0269 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1194+637_1194+638d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | ||||||
| chr5:80066094 | CA | C | 94 | a0001c0001t0001g0061 a0001c0001t0001g0103 a0001c0002t0001g0251 others(91): Show |
120 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1194+638delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | ||||||
| chr5:80066095 | A | C | 1 | a0004c0008t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1194+618A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066095 | |||||||
| chr5:80066349 | T | C | 4 | a0001c0002t0001g0269 a0001c0002t0001g0270 a0001c0002t0001g0271 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+872T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066349 | |||||||
| chr5:80066408 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1194+931C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066408 | |||||||
| chr5:80066420 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1194+943A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066420 | |||||||
| chr5:80066477 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1194+1000T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066477 | |||||||
| chr5:80066626 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1194+1149G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066626 | |||||||
| chr5:80066689 | G | T | 2 | a0001c0002t0001g0257 a0001c0002t0001g0258 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1194+1212G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066689 | |||||||
| chr5:80066690 | C | T | 1 | a0001c0002t0001g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1194+1213C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066690 | |||||||
| chr5:80066727 | G | A | 9 | a0001c0002t0001g0253 a0001c0002t0001g0264 a0001c0002t0001g0269 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195-1246G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066727 | |||||||
| chr5:80066756 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1195-1217T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066756 | |||||||
| chr5:80066789 | G | C | 44 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(41): Show |
62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1195-1184G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066789 | |||||||
| chr5:80066858 | G | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(32): Show |
38 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1195-1115G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066858 | |||||||
| chr5:80066895 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1195-1078A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066895 | |||||||
| chr5:80066926 | G | T | 1 | a0001c0002t0001g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1195-1047G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066926 | |||||||
| chr5:80067039 | G | A | 2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1195-934G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067039 | |||||||
| chr5:80067234 | T | TA | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1195-737dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80067234 | ||||||
| chr5:80067254 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1195-719C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067254 | |||||||
| chr5:80067388 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1195-585T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067388 | |||||||
| chr5:80067450 | G | A | 97 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(94): Show |
123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1195-523G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067450 | |||||||
| chr5:80067480 | G | T | 1 | a0001c0003t0001g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1195-493G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067480 | |||||||
| chr5:80067501 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0247 |
3 | HG01891.hp2 HG02145.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1195-472C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067501 | |||||||
| chr5:80067785 | C | CA | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195-187dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80067785 | ||||||
| chr5:80067936 | A | C | 2 | a0001c0003t0001g0033 a0001c0003t0001g0228 |
3 | HG00738.hp1 HG01069.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1195-37A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067936 | |||||||
| chr5:80067968 | T | C | 1 | a0001c0003t0001g0212 | 1 | NA19064.hp1 | splice_region_variant&intron_variant | LOW | c.1195-5T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067968 | |||||||
| chr5:80068200 | G | A | 1 | a0002c0004t0001g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1347+75G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068200 | |||||||
| chr5:80068492 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1347+367T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068492 | |||||||
| chr5:80068577 | T | C | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1347+452T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068577 | |||||||
| chr5:80068595 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0007c0015t0001g0024 |
3 | HG01884.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1347+470G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068595 | |||||||
| chr5:80068728 | G | A | 1 | a0001c0003t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1347+603G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068728 | |||||||
| chr5:80068751 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1347+626C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068751 | |||||||
| chr5:80068853 | A | C | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1347+728A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068853 | |||||||
| chr5:80069186 | A | G | 105 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0011 others(102): Show |
133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1347+1061A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069186 | |||||||
| chr5:80069224 | T | A | 1 | a0001c0003t0001g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1348-1082T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069224 | |||||||
| chr5:80069262 | A | G | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1348-1044A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069262 | |||||||
| chr5:80069493 | T | C | 1 | a0001c0002t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1348-813T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069493 | |||||||
| chr5:80069727 | C | G | 3 | a0005c0009t0001g0280 a0005c0009t0001g0293 a0005c0009t0001g0301 |
3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1348-579C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069727 | |||||||
| chr5:80069734 | G | T | 3 | a0002c0004t0001g0179 a0002c0004t0001g0182 a0002c0004t0001g0183 |
3 | NA18940.hp2 NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1348-572G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069734 | |||||||
| chr5:80069802 | C | T | 1 | a0002c0004t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1348-504C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069802 | |||||||
| chr5:80069836 | G | A | 1 | a0001c0002t0001g0298 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1348-470G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069836 | |||||||
| chr5:80069848 | G | A | 2 | a0001c0003t0001g0223 a0001c0003t0001g0225 |
2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1348-458G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069848 | |||||||
| chr5:80070003 | C | T | 2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1348-303C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070003 | |||||||
| chr5:80070121 | C | CT | 235 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(232): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1348-182dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 80070121 | ||||||
| chr5:80070153 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1348-153G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070153 | |||||||
| chr5:80070257 | T | C | 103 | a0001c0001t0001g0132 a0001c0001t0001g0141 a0001c0002t0001g0253 others(100): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1348-49T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070257 | |||||||
| chr5:80070303 | C | T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
splice_region_variant&intron_variant | LOW | c.1348-3C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070303 | |||||||
| chr5:80070426 | T | G | 102 | a0001c0001t0001g0064 a0001c0002t0001g0253 a0001c0002t0001g0264 others(99): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1452+16T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 11/21 | chr5 | 80070426 | |||||||
| chr5:80070790 | C | G | 1 | a0001c0002t0001g0296 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1560+40C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070790 | |||||||
| chr5:80070809 | G | A | 3 | a0001c0002t0001g0036 a0001c0002t0001g0297 a0001c0002t0001g0306 |
4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560+59G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070809 | |||||||
| chr5:80070910 | T | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0051 others(27): Show |
32 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1561-111T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070910 | |||||||
| chr5:80070936 | G | A | 1 | a0002c0004t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1561-85G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070936 | |||||||
| chr5:80071274 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1720+94G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071274 | |||||||
| chr5:80071285 | G | A | 4 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0002c0004t0001g0013 others(1): Show |
6 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+105G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071285 | |||||||
| chr5:80071655 | T | TAC | 19 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0105 others(16): Show |
22 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1720+505_1720+506d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | ||||||
| chr5:80071655 | TAC | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1720+505_1720+506d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | ||||||
| chr5:80071655 | TACAC | T | 25 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0213 others(22): Show |
27 | HG00609.hp1 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1720+503_1720+506d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | ||||||
| chr5:80071659 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1720+479C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071659 | |||||||
| chr5:80071745 | A | T | 1 | a0001c0002t0001g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1721-533A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071745 | |||||||
| chr5:80071903 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1721-375G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071903 | |||||||
| chr5:80072193 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(318): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.1721-85T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80072193 | |||||||
| chr5:80072225 | TAGA | T | 94 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0094 others(91): Show |
116 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1721-47_1721-45del others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80072225 | ||||||
| chr5:80072522 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1839+126G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072522 | |||||||
| chr5:80072569 | A | G | 127 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(124): Show |
144 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1839+173A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072569 | |||||||
| chr5:80072993 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1840-282C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072993 | |||||||
| chr5:80073155 | C | T | 1 | a0001c0003t0001g0164 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1840-120C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80073155 | |||||||
| chr5:80073226 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1840-49C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80073226 | |||||||
| chr5:80073389 | TG | T | 15 | a0001c0001t0001g0064 a0001c0002t0001g0036 a0001c0002t0001g0257 others(12): Show |
28 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1892+63delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073389 | |||||||
| chr5:80073390 | G | T | 118 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(115): Show |
132 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1892+63G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073390 | |||||||
| chr5:80073472 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1892+145T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073472 | |||||||
| chr5:80073586 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0007c0015t0001g0024 |
3 | HG01884.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1892+259A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073586 | |||||||
| chr5:80073635 | C | T | 2 | a0001c0003t0001g0316 a0001c0003t0001g0317 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1892+308C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073635 | |||||||
| chr5:80073856 | T | C | 8 | a0002c0005t0001g0012 a0002c0005t0001g0161 a0002c0005t0001g0188 others(5): Show |
10 | NA18942.hp1 NA18974.hp1 NA18988.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892+529T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073856 | |||||||
| chr5:80073857 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1892+530C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073857 | |||||||
| chr5:80074055 | C | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0062 others(10): Show |
14 | HG01361.hp1 HG02698.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1892+728C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074055 | |||||||
| chr5:80074067 | G | A | 4 | a0001c0001t0001g0132 a0001c0002t0001g0309 a0001c0010t0001g0245 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892+740G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074067 | |||||||
| chr5:80074301 | C | T | 3 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 |
3 | HG00642.hp2 HG01167.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1892+974C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074301 | |||||||
| chr5:80074386 | C | G | 1 | a0002c0004t0001g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1892+1059C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074386 | |||||||
| chr5:80074424 | G | T | 7 | a0001c0001t0001g0064 a0001c0003t0001g0002 a0001c0003t0001g0033 others(4): Show |
17 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1892+1097G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074424 | |||||||
| chr5:80074521 | C | T | 233 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(230): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1892+1194C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074521 | |||||||
| chr5:80074615 | GCTCT | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0046 |
3 | HG02615.hp2 NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1892+1297_1892+130 others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074615 | ||||||
| chr5:80074626 | C | CT | 8 | a0001c0001t0001g0077 a0001c0001t0001g0110 a0001c0001t0001g0116 others(5): Show |
10 | HG01243.hp2 HG02055.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892+1314dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | ||||||
| chr5:80074626 | C | CTT | 31 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(28): Show |
36 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1892+1313_1892+131 others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | ||||||
| chr5:80074626 | C | CTTT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG00597.hp1 HG02451.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1892+1312_1892+131 others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | ||||||
| chr5:80074626 | CT | C | 12 | a0001c0001t0001g0064 a0001c0001t0001g0088 a0001c0001t0001g0143 others(9): Show |
22 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1892+1314delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | ||||||
| chr5:80074833 | G | A | 1 | a0001c0002t0001g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1892+1506G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074833 | |||||||
| chr5:80074931 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1892+1604C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074931 | |||||||
| chr5:80074938 | TGTCCCAG others(7): Show |
T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1892+1620_1892+163 others(18): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074938 | ||||||
| chr5:80074941 | C | T | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892+1614C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074941 | |||||||
| chr5:80074952 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1892+1625G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074952 | |||||||
| chr5:80075036 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1892+1709A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075036 | |||||||
| chr5:80075043 | A | G | 131 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(128): Show |
152 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.1892+1716A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075043 | |||||||
| chr5:80075118 | A | G | 1 | a0001c0002t0001g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1893-1737A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075118 | |||||||
| chr5:80075382 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1893-1473G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075382 | |||||||
| chr5:80075424 | C | T | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1893-1431C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075424 | |||||||
| chr5:80075595 | A | G | 1 | a0001c0003t0001g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1893-1260A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075595 | |||||||
| chr5:80075900 | A | G | 1 | a0002c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1893-955A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075900 | |||||||
| chr5:80076032 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1893-823T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076032 | |||||||
| chr5:80076228 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1893-627C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076228 | |||||||
| chr5:80076584 | C | T | 226 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(223): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1893-271C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076584 | |||||||
| chr5:80076608 | T | C | 1 | a0001c0002t0001g0311 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1893-247T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076608 | |||||||
| chr5:80076645 | G | A | 2 | a0002c0004t0001g0013 a0008c0011t0001g0216 |
4 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-210G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076645 | |||||||
| chr5:80077132 | C | T | 3 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 |
3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2086+84C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077132 | |||||||
| chr5:80077212 | A | G | 2 | a0001c0003t0001g0203 a0001c0003t0001g0204 |
2 | HG00544.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2086+164A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077212 | |||||||
| chr5:80077287 | G | A | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2086+239G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077287 | |||||||
| chr5:80077461 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2086+413A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077461 | |||||||
| chr5:80077598 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2087-451G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077598 | |||||||
| chr5:80077617 | C | T | 11 | a0001c0003t0001g0032 a0001c0003t0001g0164 a0001c0003t0001g0170 others(8): Show |
12 | HG00544.hp2 NA18948.hp1 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.2087-432C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077617 | |||||||
| chr5:80077640 | G | C | 33 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
36 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2087-409G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077640 | |||||||
| chr5:80077698 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2087-351G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077698 | |||||||
| chr5:80077960 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2087-89T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077960 | |||||||
| chr5:80077980 | C | T | 135 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(132): Show |
164 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.2087-69C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077980 | |||||||
| chr5:80077989 | C | A | 2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2087-60C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077989 | |||||||
| chr5:80078012 | C | T | 1 | a0001c0003t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2087-37C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80078012 | |||||||
| chr5:80078342 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0078 |
2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2265+115G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078342 | |||||||
| chr5:80078468 | C | T | 2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2265+241C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078468 | |||||||
| chr5:80078556 | C | T | 40 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0003t0001g0004 others(37): Show |
50 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2265+329C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078556 | |||||||
| chr5:80078650 | T | C | 1 | a0001c0003t0001g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2266-271T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078650 | |||||||
| chr5:80078658 | A | T | 1 | a0001c0002t0001g0252 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2266-263A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078658 | |||||||
| chr5:80078765 | A | C | 1 | a0002c0004t0001g0030 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2266-156A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078765 | |||||||
| chr5:80078784 | AT | A | 131 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(128): Show |
160 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.2266-134delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 80078784 | ||||||
| chr5:80078858 | A | T | 1 | a0001c0002t0001g0302 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2266-63A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078858 | |||||||
| chr5:80079435 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0309 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2511+177A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079435 | |||||||
| chr5:80079691 | CATGGAAT others(5): Show |
C | 1 | a0001c0003t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2512-206_2512-195d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 80079691 | ||||||
| chr5:80079752 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0072 others(10): Show |
15 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.2512-153T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079752 | |||||||
| chr5:80079772 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2512-133T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079772 | |||||||
| chr5:80079868 | T | TGTCCTGT others(4): Show |
1 | a0001c0003t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2512-36_2512-26dup others(11): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 80079868 | ||||||
| chr5:80079889 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2512-16T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079889 | |||||||
| chr5:80079901 | G | C | 133 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(130): Show |
162 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(159): Show |
splice_region_variant&intron_variant | LOW | c.2512-4G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079901 | |||||||
| chr5:80080112 | G | A | 1 | a0001c0003t0001g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2684+35G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080112 | |||||||
| chr5:80080128 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2684+51C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080128 | |||||||
| chr5:80080321 | G | A | 2 | a0001c0001t0001g0132 a0001c0002t0001g0309 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2684+244G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080321 | |||||||
| chr5:80080408 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0072 others(9): Show |
14 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.2684+331G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080408 | |||||||
| chr5:80080509 | TGCA | T | 231 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(228): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.2684+436_2684+438d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080509 | ||||||
| chr5:80080565 | A | G | 232 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(229): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2684+488A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080565 | |||||||
| chr5:80080577 | A | ATTTTTTT others(7): Show |
1 | a0002c0004t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2684+501_2684+502i others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080577 | ||||||
| chr5:80080579 | C | CT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0001g0247 others(3): Show |
7 | HG01070.hp2 HG01952.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.2684+527dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0144 a0001c0001t0001g0148 others(2): Show |
6 | HG00673.hp1 HG02074.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2684+525_2684+527d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(4): Show |
1 | a0005c0009t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2684+517_2684+527d others(13): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(6): Show |
20 | a0001c0002t0001g0264 a0001c0002t0001g0269 a0001c0003t0001g0223 others(17): Show |
23 | HG00099.hp2 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2684+515_2684+527d others(15): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(7): Show |
27 | a0001c0001t0001g0104 a0001c0002t0001g0270 a0001c0002t0001g0273 others(24): Show |
33 | HG00609.hp2 HG00642.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2684+514_2684+527d others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(8): Show |
17 | a0001c0002t0001g0241 a0001c0002t0001g0271 a0001c0002t0001g0274 others(14): Show |
19 | HG00140.hp1 HG00408.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2684+513_2684+527d others(17): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(9): Show |
14 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0299 others(11): Show |
16 | HG00140.hp2 HG00673.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2684+512_2684+527d others(18): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(10): Show |
11 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0156 others(8): Show |
11 | HG00609.hp1 HG00741.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2684+511_2684+527d others(19): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(11): Show |
12 | a0001c0002t0001g0135 a0001c0002t0001g0137 a0001c0002t0001g0151 others(9): Show |
12 | HG01167.hp2 HG01952.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.2684+510_2684+527d others(20): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(12): Show |
14 | a0001c0002t0001g0008 a0001c0002t0001g0138 a0001c0002t0001g0139 others(11): Show |
19 | HG00544.hp2 HG00642.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2684+509_2684+527d others(21): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(13): Show |
14 | a0001c0001t0001g0018 a0001c0002t0001g0015 a0001c0002t0001g0037 others(11): Show |
18 | HG00597.hp2 HG01891.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.2684+508_2684+527d others(22): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(14): Show |
13 | a0001c0002t0001g0016 a0001c0002t0001g0136 a0001c0002t0001g0252 others(10): Show |
15 | HG00733.hp2 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2684+507_2684+527d others(23): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0056 a0001c0002t0001g0304 a0001c0002t0001g0305 others(1): Show |
5 | HG02071.hp2 HG03704.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2684+506_2684+527d others(24): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0058 a0001c0002t0001g0260 a0002c0007t0002g0159 |
3 | HG00597.hp1 HG02559.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2684+505_2684+527d others(25): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0052 a0001c0002t0001g0277 a0001c0002t0001g0292 |
3 | HG02040.hp2 HG02615.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2684+504_2684+527d others(26): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0060 a0001c0003t0001g0206 |
2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2684+503_2684+527d others(27): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0094 others(1): Show |
4 | HG02056.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(28): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0114 others(1): Show |
5 | HG02129.hp2 HG02735.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(29): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0071 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG00621.hp2 NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(30): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(22): Show |
6 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0106 others(3): Show |
6 | HG01123.hp2 HG02818.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(31): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0107 a0001c0001t0001g0121 a0001c0003t0001g0170 |
3 | HG02300.hp1 NA18948.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(32): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0150 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2684+527_2684+528i others(35): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2684+527_2684+528i others(36): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | C | T | 1 | a0002c0004t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2684+502C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080579 | |||||||
| chr5:80080579 | CT | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0084 others(7): Show |
10 | HG02132.hp1 HG03486.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.2684+527delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080579 | CTT | C | 13 | a0001c0002t0001g0036 a0001c0002t0001g0257 a0001c0002t0001g0258 others(10): Show |
26 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2684+526_2684+527d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | ||||||
| chr5:80080588 | T | TTTTTTTT others(10): Show |
2 | a0001c0002t0001g0285 a0001c0002t0001g0286 |
2 | HG00438.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(19): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080588 | ||||||
| chr5:80080691 | A | T | 125 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(122): Show |
144 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.2684+614A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080691 | |||||||
| chr5:80080735 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2684+658C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080735 | |||||||
| chr5:80080736 | G | A | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2684+659G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080736 | |||||||
| chr5:80080743 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2684+666C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080743 | |||||||
| chr5:80080744 | G | A | 9 | a0001c0003t0001g0140 a0001c0003t0001g0165 a0001c0003t0001g0166 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2684+667G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080744 | |||||||
| chr5:80080993 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2684+916T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080993 | |||||||
| chr5:80081082 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2684+1005T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081082 | |||||||
| chr5:80081140 | G | A | 1 | a0001c0003t0001g0192 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2684+1063G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081140 | |||||||
| chr5:80081211 | A | T | 1 | a0001c0002t0001g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2684+1134A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081211 | |||||||
| chr5:80081308 | C | T | 3 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0003t0001g0237 |
3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2685-1098C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081308 | |||||||
| chr5:80081347 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2685-1059C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081347 | |||||||
| chr5:80081410 | G | A | 1 | a0001c0002t0001g0290 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2685-996G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081410 | |||||||
| chr5:80081426 | A | G | 48 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0016 others(45): Show |
55 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.2685-980A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081426 | |||||||
| chr5:80081532 | C | T | 1 | a0002c0004t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2685-874C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081532 | |||||||
| chr5:80081750 | T | C | 1 | a0001c0003t0001g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2685-656T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081750 | |||||||
| chr5:80082018 | G | GGTA | 4 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0002c0004t0001g0013 others(1): Show |
6 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685-387_2685-385d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80082018 | ||||||
| chr5:80082033 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2685-373C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082033 | |||||||
| chr5:80082077 | G | T | 232 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(229): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2685-329G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082077 | |||||||
| chr5:80082114 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2685-292A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082114 | |||||||
| chr5:80082204 | A | G | 3 | a0001c0002t0001g0269 a0001c0002t0001g0271 a0001c0002t0001g0274 |
3 | HG00099.hp2 HG00140.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.2685-202A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082204 | |||||||
| chr5:80082247 | C | G | 232 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(229): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2685-159C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082247 | |||||||
| chr5:80082311 | A | G | 2 | a0001c0001t0001g0061 a0001c0003t0001g0205 |
2 | HG00558.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2685-95A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082311 | |||||||
| chr5:80082624 | T | TC | 85 | a0001c0001t0001g0094 a0001c0002t0001g0008 a0001c0002t0001g0015 others(82): Show |
98 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2824+86dupC | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082624 | ||||||
| chr5:80082686 | C | A | 1 | a0002c0004t0001g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2824+141C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082686 | |||||||
| chr5:80082705 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2824+160A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082705 | |||||||
| chr5:80082812 | A | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2824+267A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082812 | |||||||
| chr5:80082839 | T | TAATC | 3 | a0005c0009t0001g0280 a0005c0009t0001g0293 a0005c0009t0001g0301 |
3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2825-239_2825-236d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082839 | ||||||
| chr5:80082960 | TGCGGGGC others(7): Show |
T | 94 | a0001c0001t0001g0046 a0001c0001t0001g0094 a0001c0002t0001g0008 others(91): Show |
110 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2825-114_2825-101d others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082960 | ||||||
| chr5:80083002 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2825-78G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80083002 |