Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55901 |
| ensemblid | ENSG00000136114.17 |
| hgncid | 17754 |
| symbol | THSD1 |
| name | thrombospondin type 1 domain containing 1 |
| refseq_nuc | NM_018676.4 |
| refseq_prot | NP_061146.1 |
| ensembl_nuc | ENST00000258613.5 |
| ensembl_prot | ENSP00000258613.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 52377167 |
| end | 52406172 |
| strand | - |
| ver | v1.2 |
| region | chr13:52377167-52406172 |
| region5000 | chr13:52372167-52411172 |
| regionname0 | THSD1_chr13_52377167_52406172 |
| regionname5000 | THSD1_chr13_52372167_52411172 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 852 | 282 | 59 | 55 | 127 | 9 | 30 | 91 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0002 | 0/0 | 852 | 7 | 0 | 1 | 4 | 0 | 2 | 3 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0003 | 0/0 | 852 | 6 | 4 | 1 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0004 | 0/0 | 852 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0005 | 0/0 | 852 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0006 | 0/0 | 852 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0007 | 0/0 | 852 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0008 | 0/0 | 852 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0009 | 0/0 | 852 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0010 | 0/0 | 852 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0011 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| a0012 | 0/0 | 852 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | MKPML others(847): Show |
chr13 | 52372167 | 52411172 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2556 | 146 | 23 | 36 | 71 | 4 | 12 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0002 | 1/1 | 2556 | 123 | 29 | 19 | 51 | 5 | 17 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0007 | 0/0 | 2556 | 3 | 0 | 0 | 3 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0009 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0011 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0012 | 0/0 | 2556 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0015 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0017 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0001c0018 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0002c0003 | 0/0 | 2556 | 7 | 0 | 1 | 4 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0003c0004 | 0/0 | 2556 | 6 | 4 | 1 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0004c0006 | 0/0 | 2556 | 4 | 4 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0004c0020 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0005c0005 | 0/0 | 2556 | 4 | 3 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0006c0008 | 0/0 | 2556 | 3 | 0 | 0 | 3 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0007c0013 | 0/0 | 2556 | 2 | 0 | 0 | 1 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0008c0010 | 0/0 | 2556 | 2 | 0 | 0 | 0 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0009c0014 | 0/0 | 2556 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0010c0016 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0011c0019 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 | ||
| a0012c0021 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | ATGAA others(2551): Show |
chr13 | 52372167 | 52411172 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3026 | 144 | 21 | 36 | 71 | 4 | 12 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0001t0004 | 0/0 | 3026 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0002t0001 | 1/1 | 3026 | 121 | 28 | 19 | 50 | 5 | 17 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0002t0005 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0002t0006 | 0/0 | 3026 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0007t0001 | 0/0 | 3026 | 3 | 0 | 0 | 3 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0009t0001 | 0/0 | 3026 | 3 | 3 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0011t0001 | 0/0 | 3026 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0012t0001 | 0/0 | 3026 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0015t0001 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0017t0001 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0001c0018t0001 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0002c0003t0003 | 0/0 | 3026 | 7 | 0 | 1 | 4 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0003c0004t0001 | 0/0 | 3026 | 3 | 2 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0003c0004t0002 | 0/0 | 3026 | 3 | 2 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0004c0006t0001 | 0/0 | 3026 | 4 | 4 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0004c0020t0001 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0005c0005t0002 | 0/0 | 3026 | 4 | 3 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0006c0008t0001 | 0/0 | 3026 | 3 | 0 | 0 | 3 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0007c0013t0001 | 0/0 | 3026 | 2 | 0 | 0 | 1 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0008c0010t0001 | 0/0 | 3026 | 2 | 0 | 0 | 0 | 0 | 2 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0009c0014t0001 | 0/0 | 3026 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0010c0016t0001 | 0/0 | 3026 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0011c0019t0002 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| a0012c0021t0001 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | GTGGG others(3021): Show |
chr13 | 52372167 | 52411172 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 23 | 1 | 5 | 9 | 2 | 6 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0003 | 0/0 | 21 | 0 | 0 | 20 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0001 | 0/0 | 31 | 5 | 4 | 21 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0004 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0005 | 0/0 | 5 | 2 | 1 | 0 | 1 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0013 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0016 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0002t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0007t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0009t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0009t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0011t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0012t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0012t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0015t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0017t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0001c0018t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0002c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0003c0004t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0003c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0003c0004t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0003c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0004c0006t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0004c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0004c0006t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0004c0020t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0005c0005t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0005c0005t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0005c0005t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0005c0005t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0006c0008t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0007c0013t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0007c0013t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0008c0010t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0008c0010t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0009c0014t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0009c0014t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0010c0016t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0011c0019t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| a0012c0021t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0030 | EUR | GBR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00408 | hp1 | a0006 | c0008 | t0001 | g0011 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00544 | hp2 | a0002 | c0003 | t0003 | g0187 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01099 | hp1 | a0002 | c0003 | t0003 | g0038 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01243 | hp1 | a0005 | c0005 | t0002 | g0182 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01243 | hp2 | a0003 | c0004 | t0001 | g0014 | AMR | PUR | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0046 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02056 | hp2 | a0007 | c0013 | t0001 | g0150 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02080 | hp2 | a0001 | c0007 | t0001 | g0082 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02083 | hp2 | a0010 | c0016 | t0001 | g0126 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02257 | hp2 | a0001 | c0009 | t0001 | g0048 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02280 | hp1 | a0001 | c0017 | t0001 | g0087 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0041 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02615 | hp1 | a0004 | c0020 | t0001 | g0172 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02622 | hp1 | a0001 | c0011 | t0001 | g0031 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02630 | hp1 | a0004 | c0006 | t0001 | g0173 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02886 | hp1 | a0005 | c0005 | t0002 | g0183 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02896 | hp1 | a0001 | c0018 | t0001 | g0143 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02922 | hp1 | a0004 | c0006 | t0001 | g0037 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02970 | hp2 | a0011 | c0019 | t0002 | g0178 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03017 | hp1 | a0008 | c0010 | t0001 | g0167 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0189 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03130 | hp2 | a0004 | c0006 | t0001 | g0037 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03139 | hp1 | a0001 | c0011 | t0001 | g0031 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03486 | hp2 | a0005 | c0005 | t0002 | g0184 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03669 | hp2 | a0008 | c0010 | t0001 | g0148 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03688 | hp1 | a0002 | c0003 | t0003 | g0038 | SAS | STU | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG03942 | hp2 | a0007 | c0013 | t0001 | g0084 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG04184 | hp2 | a0001 | c0015 | t0001 | g0125 | SAS | BEB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | STU | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | STU | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18522 | hp2 | a0003 | c0004 | t0002 | g0179 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18906 | hp1 | a0005 | c0005 | t0002 | g0185 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18941 | hp2 | a0006 | c0008 | t0001 | g0011 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18969 | hp2 | a0009 | c0014 | t0001 | g0141 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18991 | hp1 | a0006 | c0008 | t0001 | g0011 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18993 | hp1 | a0001 | c0007 | t0001 | g0113 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0188 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18997 | hp2 | a0001 | c0007 | t0001 | g0140 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19030 | hp1 | a0004 | c0006 | t0001 | g0171 | AFR | LWK | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | LWK | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0165 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19065 | hp2 | a0001 | c0012 | t0001 | g0093 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19067 | hp1 | a0001 | c0012 | t0001 | g0063 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19067 | hp2 | a0009 | c0014 | t0001 | g0142 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0186 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19082 | hp1 | a0002 | c0003 | t0003 | g0190 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0014 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | YRI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ASW | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0138 | EUR | TSI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20752 | hp2 | a0012 | c0021 | t0001 | g0098 | EUR | TSI | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20905 | hp2 | a0003 | c0004 | t0002 | g0181 | SAS | GIH | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02109 | hp2 | a0001 | c0009 | t0001 | g0047 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0180 | AFR | USA | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | USA | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | USA | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0014 | AFR | USA | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0016 | REF | REF | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0072 | REF | REF | THSD1_chr13_52372167_52411172 | THSD1 | chr13 | 52372167 | 52411172 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52377431 | C | T | 1 | a0010 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.2539G>A | p.Val847Met | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2762/3026 | 2539/2559 | 847/852 | chr13 | 52377431 | |||
| chr13:52377667 | T | C | 1 | a0002 | 7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
missense_variant | MODERATE | c.2303A>G | p.Lys768Arg | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2526/3026 | 2303/2559 | 768/852 | chr13 | 52377667 | |||
| chr13:52377889 | C | A | 2 | a0003 a0011 |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
missense_variant | MODERATE | c.2081G>T | p.Arg694Ile | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2304/3026 | 2081/2559 | 694/852 | chr13 | 52377889 | |||
| chr13:52377916 | G | T | 1 | a0007 | 2 | HG02056.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.2054C>A | p.Thr685Lys | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2277/3026 | 2054/2559 | 685/852 | chr13 | 52377916 | |||
| chr13:52378499 | C | G | 3 | a0003 a0005 a0011 |
11 | HG01243.hp1 HG01243.hp2 HG02886.hp1 others(8): Show |
missense_variant | MODERATE | c.1471G>C | p.Asp491His | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1694/3026 | 1471/2559 | 491/852 | chr13 | 52378499 | |||
| chr13:52378555 | C | T | 1 | a0006 | 3 | HG00408.hp1 NA18941.hp2 NA18991.hp1 |
missense_variant | MODERATE | c.1415G>A | p.Ser472Asn | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1638/3026 | 1415/2559 | 472/852 | chr13 | 52378555 | |||
| chr13:52386085 | G | A | 1 | a0011 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1123C>T | p.Pro375Ser | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/5 | 1346/3026 | 1123/2559 | 375/852 | chr13 | 52386085 | |||
| chr13:52397382 | C | T | 1 | a0008 | 2 | HG03017.hp1 HG03669.hp2 |
missense_variant | MODERATE | c.871G>A | p.Glu291Lys | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 1094/3026 | 871/2559 | 291/852 | chr13 | 52397382 | |||
| chr13:52397583 | G | C | 3 | a0002 a0004 a0005 |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
missense_variant | MODERATE | c.670C>G | p.Arg224Gly | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 893/3026 | 670/2559 | 224/852 | chr13 | 52397583 | |||
| chr13:52397661 | G | C | 1 | a0012 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.592C>G | p.Gln198Glu | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 815/3026 | 592/2559 | 198/852 | chr13 | 52397661 | |||
| chr13:52397915 | G | A | 1 | a0009 | 2 | NA18969.hp2 NA19067.hp2 |
missense_variant | MODERATE | c.338C>T | p.Pro113Leu | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 561/3026 | 338/2559 | 113/852 | chr13 | 52397915 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52378179 | G | A | 1 | a0001c0018 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.1791C>T | p.Val597Val | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2014/3026 | 1791/2559 | 597/852 | chr13 | 52378179 | |||
| chr13:52378182 | C | G | 1 | a0004c0006 | 4 | HG02630.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.1788G>C | p.Ala596Ala | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2011/3026 | 1788/2559 | 596/852 | chr13 | 52378182 | |||
| chr13:52378182 | C | T | 1 | a0001c0017 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1788G>A | p.Ala596Ala | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 2011/3026 | 1788/2559 | 596/852 | chr13 | 52378182 | |||
| chr13:52378256 | A | G | 2 | a0001c0009 a0004c0020 |
4 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
synonymous_variant | LOW | c.1714T>C | p.Leu572Leu | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1937/3026 | 1714/2559 | 572/852 | chr13 | 52378256 | |||
| chr13:52378362 | C | T | 1 | a0001c0012 | 2 | NA19065.hp2 NA19067.hp1 |
synonymous_variant | LOW | c.1608G>A | p.Gln536Gln | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1831/3026 | 1608/2559 | 536/852 | chr13 | 52378362 | |||
| chr13:52378440 | G | A | 5 | a0001c0009 a0002c0003 a0004c0006 others(2): Show |
19 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(16): Show |
synonymous_variant | LOW | c.1530C>T | p.Ala510Ala | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1753/3026 | 1530/2559 | 510/852 | chr13 | 52378440 | |||
| chr13:52378545 | G | A | 3 | a0002c0003 a0004c0006 a0005c0005 |
15 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(12): Show |
synonymous_variant | LOW | c.1425C>T | p.Arg475Arg | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1648/3026 | 1425/2559 | 475/852 | chr13 | 52378545 | |||
| chr13:52378638 | C | T | 1 | a0001c0015 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1332G>A | p.Lys444Lys | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 5/5 | 1555/3026 | 1332/2559 | 444/852 | chr13 | 52378638 | |||
| chr13:52397395 | G | A | 1 | a0001c0011 | 2 | HG02622.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.858C>T | p.Thr286Thr | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 1081/3026 | 858/2559 | 286/852 | chr13 | 52397395 | |||
| chr13:52397437 | G | A | 1 | a0011c0019 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.816C>T | p.Val272Val | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 1039/3026 | 816/2559 | 272/852 | chr13 | 52397437 | |||
| chr13:52397734 | G | A | 2 | a0001c0007 a0009c0014 |
5 | HG02080.hp2 NA18969.hp2 NA18993.hp1 others(2): Show |
synonymous_variant | LOW | c.519C>T | p.Asn173Asn | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 742/3026 | 519/2559 | 173/852 | chr13 | 52397734 | |||
| chr13:52397758 | G | A | 14 | a0001c0001 a0001c0009 a0001c0012 others(11): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
synonymous_variant | LOW | c.495C>T | p.Ile165Ile | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/5 | 718/3026 | 495/2559 | 165/852 | chr13 | 52397758 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52402644 | T | C | 1 | a0001c0002t0006 | 1 | NA19056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/5 | 44 | chr13 | 52402644 | ||||||
| chr13:52406082 | C | T | 1 | a0001c0002t0005 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-133G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/5 | 3482 | chr13 | 52406082 | ||||||
| chr13:52406084 | G | A | 1 | a0002c0003t0003 | 7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-135C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/5 | 3484 | chr13 | 52406084 | ||||||
| chr13:52406093 | G | C | 4 | a0002c0003t0003 a0003c0004t0002 a0005c0005t0002 others(1): Show |
15 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-144C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/5 | 3493 | chr13 | 52406093 | ||||||
| chr13:52406116 | G | T | 1 | a0001c0001t0004 | 2 | HG02145.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-167C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/5 | 3516 | chr13 | 52406116 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52378793 | CA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(164): Show |
splice_region_variant&intron_variant | LOW | c.1181-5delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378793 | |||||||
| chr13:52378798 | A | C | 2 | a0001c0002t0001g0077 a0003c0004t0002g0179 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1181-9T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378798 | |||||||
| chr13:52378863 | C | CT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0071 others(14): Show |
19 | HG00423.hp1 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1181-75dupA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378863 | |||||||
| chr13:52378863 | CT | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0045 others(22): Show |
29 | HG00544.hp2 HG01069.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1181-75delA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378863 | |||||||
| chr13:52378863 | CTT | C | 6 | a0001c0001t0001g0069 a0003c0004t0001g0014 a0003c0004t0002g0179 others(3): Show |
8 | HG01243.hp2 HG02897.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-76_1181-75del others(2): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378863 | |||||||
| chr13:52378978 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1181-189A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52378978 | |||||||
| chr13:52379023 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1181-234A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379023 | |||||||
| chr13:52379107 | C | A | 3 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 |
4 | HG02630.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-318G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379107 | |||||||
| chr13:52379115 | G | T | 1 | a0001c0002t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1181-326C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379115 | |||||||
| chr13:52379472 | T | C | 1 | a0001c0002t0001g0029 | 2 | HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1181-683A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379472 | |||||||
| chr13:52379506 | C | T | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-717G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379506 | |||||||
| chr13:52379587 | G | A | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181-798C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379587 | |||||||
| chr13:52379632 | C | G | 15 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0189 others(12): Show |
19 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1181-843G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379632 | |||||||
| chr13:52379661 | A | G | 28 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0045 others(25): Show |
34 | HG00544.hp2 HG01099.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1181-872T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379661 | |||||||
| chr13:52379686 | G | T | 2 | a0004c0006t0001g0173 a0004c0020t0001g0172 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1181-897C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379686 | |||||||
| chr13:52379689 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0009t0001g0046 others(2): Show |
6 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181-900C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379689 | |||||||
| chr13:52379765 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1181-976C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379765 | |||||||
| chr13:52379813 | T | C | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-1024A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379813 | |||||||
| chr13:52379822 | G | A | 1 | a0001c0002t0006g0165 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1181-1033C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379822 | |||||||
| chr13:52379893 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0064 a0001c0001t0001g0099 others(1): Show |
5 | NA18974.hp1 NA18978.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181-1104C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52379893 | |||||||
| chr13:52380063 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1181-1274A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380063 | |||||||
| chr13:52380079 | C | T | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181-1290G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380079 | |||||||
| chr13:52380234 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0111 |
2 | HG01074.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1181-1445G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380234 | |||||||
| chr13:52380265 | C | T | 2 | a0001c0001t0001g0065 a0012c0021t0001g0098 |
2 | HG01069.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1181-1476G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380265 | |||||||
| chr13:52380297 | A | G | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-1508T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380297 | |||||||
| chr13:52380330 | T | TC | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(76): Show |
138 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1181-1542dupG | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380330 | |||||||
| chr13:52380511 | C | CT | 8 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0009t0001g0047 others(5): Show |
10 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1181-1723dupA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380511 | |||||||
| chr13:52380603 | C | T | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181-1814G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380603 | |||||||
| chr13:52380615 | T | C | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-1826A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380615 | |||||||
| chr13:52380670 | G | A | 5 | a0001c0002t0001g0016 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
5 | HG02970.hp2 HG03654.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181-1881C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380670 | |||||||
| chr13:52380850 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1181-2061G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380850 | |||||||
| chr13:52380996 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1181-2207G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52380996 | |||||||
| chr13:52381279 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1181-2490T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381279 | |||||||
| chr13:52381312 | T | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0009t0001g0046 others(2): Show |
6 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181-2523A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381312 | |||||||
| chr13:52381364 | T | A | 1 | a0003c0004t0001g0014 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1181-2575A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381364 | |||||||
| chr13:52381499 | A | G | 2 | a0001c0002t0001g0123 a0001c0002t0001g0166 |
2 | HG00544.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1181-2710T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381499 | |||||||
| chr13:52381637 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0153 |
4 | HG01952.hp2 NA18968.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-2848T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381637 | |||||||
| chr13:52381764 | T | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(111): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1181-2975A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381764 | |||||||
| chr13:52381813 | A | T | 1 | a0004c0006t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1181-3024T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381813 | |||||||
| chr13:52381992 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1181-3203A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52381992 | |||||||
| chr13:52382055 | A | C | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-3266T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382055 | |||||||
| chr13:52382139 | T | G | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-3350A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382139 | |||||||
| chr13:52382229 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(1): Show |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-3440G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382229 | |||||||
| chr13:52382514 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1180+3514C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382514 | |||||||
| chr13:52382560 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG00621.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1180+3468A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382560 | |||||||
| chr13:52382630 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1180+3398T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382630 | |||||||
| chr13:52382722 | C | T | 14 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(11): Show |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180+3306G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382722 | |||||||
| chr13:52382819 | G | A | 2 | a0001c0002t0001g0010 a0001c0002t0001g0074 |
4 | HG03490.hp1 HG03492.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+3209C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382819 | |||||||
| chr13:52382852 | C | A | 14 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(11): Show |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180+3176G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382852 | |||||||
| chr13:52382933 | C | T | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+3095G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52382933 | |||||||
| chr13:52383000 | CA | C | 15 | a0001c0002t0001g0121 a0002c0003t0003g0038 a0002c0003t0003g0186 others(12): Show |
17 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1180+3027delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383000 | |||||||
| chr13:52383055 | T | G | 1 | a0001c0002t0001g0128 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1180+2973A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383055 | |||||||
| chr13:52383093 | A | C | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+2935T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383093 | |||||||
| chr13:52383094 | T | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0009t0001g0046 others(2): Show |
6 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+2934A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383094 | |||||||
| chr13:52383385 | T | G | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+2643A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383385 | |||||||
| chr13:52383653 | G | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1180+2375C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383653 | |||||||
| chr13:52383729 | A | G | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1180+2299T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383729 | |||||||
| chr13:52383944 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0064 a0001c0001t0001g0088 others(3): Show |
7 | NA18956.hp2 NA18974.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+2084A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52383944 | |||||||
| chr13:52384086 | G | A | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+1942C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384086 | |||||||
| chr13:52384117 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1180+1911C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384117 | |||||||
| chr13:52384184 | C | CA | 20 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0054 others(17): Show |
22 | HG01069.hp1 HG01175.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1180+1843dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384184 | |||||||
| chr13:52384184 | CA | C | 7 | a0001c0001t0001g0169 a0001c0001t0004g0040 a0001c0002t0001g0013 others(4): Show |
9 | HG01071.hp1 HG02895.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180+1843delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384184 | |||||||
| chr13:52384203 | AG | A | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1824delC | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384203 | |||||||
| chr13:52384204 | G | A | 13 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(10): Show |
16 | HG01243.hp1 HG01243.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180+1824C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384204 | |||||||
| chr13:52384207 | G | A | 3 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 |
3 | HG06807.hp1 NA18522.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1180+1821C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384207 | |||||||
| chr13:52384554 | G | A | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+1474C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384554 | |||||||
| chr13:52384609 | T | C | 1 | a0005c0005t0002g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1180+1419A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384609 | |||||||
| chr13:52384653 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1180+1375A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384653 | |||||||
| chr13:52384760 | T | G | 14 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(11): Show |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180+1268A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384760 | |||||||
| chr13:52384936 | G | GA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(10): Show |
15 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1180+1091dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384936 | |||||||
| chr13:52384936 | GA | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0068 others(8): Show |
14 | HG01074.hp2 HG01192.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1180+1091delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52384936 | |||||||
| chr13:52385088 | G | A | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1180+940C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385088 | |||||||
| chr13:52385295 | C | T | 1 | a0005c0005t0002g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1180+733G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385295 | |||||||
| chr13:52385367 | C | G | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+661G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385367 | |||||||
| chr13:52385392 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1180+636G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385392 | |||||||
| chr13:52385446 | C | T | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180+582G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385446 | |||||||
| chr13:52385447 | G | A | 1 | a0005c0005t0002g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1180+581C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385447 | |||||||
| chr13:52385448 | A | AGTAT | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+576_1180+579d others(6): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385448 | |||||||
| chr13:52385465 | T | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1180+563A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385465 | |||||||
| chr13:52385495 | C | T | 2 | a0001c0002t0001g0010 a0001c0002t0001g0074 |
4 | HG03490.hp1 HG03492.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+533G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385495 | |||||||
| chr13:52385557 | CAGGGTAT | C | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+464_1180+470d others(9): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385557 | |||||||
| chr13:52385572 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1180+456C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385572 | |||||||
| chr13:52385700 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(111): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1180+327dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385700 | |||||||
| chr13:52385922 | G | T | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1180+106C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52385922 | |||||||
| chr13:52386006 | C | T | 2 | a0001c0001t0001g0056 a0003c0004t0002g0180 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1180+22G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 4/4 | chr13 | 52386006 | |||||||
| chr13:52386274 | C | T | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1022-88G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52386274 | |||||||
| chr13:52386377 | G | A | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1022-191C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52386377 | |||||||
| chr13:52386397 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(1): Show |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022-211G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52386397 | |||||||
| chr13:52386574 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(111): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1022-388C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52386574 | |||||||
| chr13:52387086 | T | C | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1022-900A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387086 | |||||||
| chr13:52387116 | T | C | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1022-930A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387116 | |||||||
| chr13:52387131 | G | T | 3 | a0001c0009t0001g0046 a0001c0009t0001g0047 a0001c0009t0001g0048 |
3 | HG01891.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1022-945C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387131 | |||||||
| chr13:52387235 | C | G | 1 | a0001c0002t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1022-1049G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387235 | |||||||
| chr13:52387242 | T | C | 2 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1022-1056A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387242 | |||||||
| chr13:52387261 | T | C | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-1075A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387261 | |||||||
| chr13:52387295 | A | G | 1 | a0001c0002t0001g0030 | 2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1022-1109T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387295 | |||||||
| chr13:52387358 | A | G | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-1172T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387358 | |||||||
| chr13:52387519 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1022-1333A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387519 | |||||||
| chr13:52387706 | G | T | 2 | a0005c0005t0002g0182 a0005c0005t0002g0184 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1022-1520C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387706 | |||||||
| chr13:52387720 | G | A | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-1534C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387720 | |||||||
| chr13:52387776 | C | CA | 4 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0066 others(1): Show |
5 | HG01106.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022-1591dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387776 | |||||||
| chr13:52387962 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1022-1776G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387962 | |||||||
| chr13:52387978 | T | C | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-1792A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52387978 | |||||||
| chr13:52388046 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0081 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1022-1860G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388046 | |||||||
| chr13:52388135 | G | T | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1022-1949C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388135 | |||||||
| chr13:52388191 | A | AT | 18 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(15): Show |
22 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1022-2006_1022-200 others(5): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388191 | |||||||
| chr13:52388191 | A | T | 1 | a0005c0005t0002g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1022-2005T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388191 | |||||||
| chr13:52388234 | A | G | 2 | a0005c0005t0002g0183 a0005c0005t0002g0185 |
2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1022-2048T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388234 | |||||||
| chr13:52388392 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1022-2206A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388392 | |||||||
| chr13:52388500 | C | CA | 2 | a0001c0001t0001g0017 a0001c0001t0001g0045 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1022-2315dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388500 | |||||||
| chr13:52388555 | C | T | 1 | a0004c0006t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1022-2369G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388555 | |||||||
| chr13:52388568 | C | T | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-2382G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388568 | |||||||
| chr13:52388582 | C | T | 14 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(11): Show |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1022-2396G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388582 | |||||||
| chr13:52388604 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0069 |
3 | HG02486.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1022-2418G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388604 | |||||||
| chr13:52388751 | G | A | 1 | a0005c0005t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1022-2565C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388751 | |||||||
| chr13:52388841 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1022-2655C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388841 | |||||||
| chr13:52388966 | C | CTT | 9 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(6): Show |
11 | HG01243.hp1 HG01243.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022-2782_1022-278 others(6): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388966 | |||||||
| chr13:52388966 | C | CTTT | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-2783_1022-278 others(7): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52388966 | |||||||
| chr13:52389086 | A | G | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-2900T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389086 | |||||||
| chr13:52389255 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1022-3069C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389255 | |||||||
| chr13:52389353 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1022-3167T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389353 | |||||||
| chr13:52389477 | T | C | 1 | a0001c0002t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1022-3291A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389477 | |||||||
| chr13:52389497 | AT | A | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-3312delA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389497 | |||||||
| chr13:52389576 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0045 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1022-3390T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389576 | |||||||
| chr13:52389825 | C | A | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1022-3639G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389825 | |||||||
| chr13:52389848 | T | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
10 | HG01106.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1022-3662A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389848 | |||||||
| chr13:52389874 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0111 |
2 | HG01074.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1022-3688G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389874 | |||||||
| chr13:52389971 | C | T | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-3785G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389971 | |||||||
| chr13:52389976 | C | A | 1 | a0001c0002t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1022-3790G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52389976 | |||||||
| chr13:52390140 | C | CA | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(84): Show |
148 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1022-3955dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390140 | |||||||
| chr13:52390140 | C | CAA | 16 | a0001c0001t0001g0033 a0001c0001t0001g0067 a0001c0001t0001g0095 others(13): Show |
21 | HG00438.hp2 HG00544.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1022-3956_1022-395 others(6): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390140 | |||||||
| chr13:52390140 | C | CAAA | 7 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 others(4): Show |
7 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-3957_1022-395 others(7): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390140 | |||||||
| chr13:52390161 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02083.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1022-3975A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390161 | |||||||
| chr13:52390180 | C | T | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-3994G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390180 | |||||||
| chr13:52390593 | A | T | 1 | a0001c0009t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1022-4407T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390593 | |||||||
| chr13:52390693 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1022-4507G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390693 | |||||||
| chr13:52390834 | C | A | 1 | a0003c0004t0001g0014 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1022-4648G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390834 | |||||||
| chr13:52390837 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1022-4651A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390837 | |||||||
| chr13:52390846 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1022-4660A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52390846 | |||||||
| chr13:52391162 | C | T | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1022-4976G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391162 | |||||||
| chr13:52391220 | A | AT | 12 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0169 others(9): Show |
14 | HG00544.hp2 HG00621.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1022-5035dupA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391220 | |||||||
| chr13:52391220 | AT | A | 6 | a0003c0004t0001g0014 a0005c0005t0002g0182 a0005c0005t0002g0183 others(3): Show |
8 | HG01243.hp1 HG01243.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-5035delA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391220 | |||||||
| chr13:52391287 | C | G | 14 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(11): Show |
16 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1022-5101G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391287 | |||||||
| chr13:52391525 | TATATATA others(11): Show |
T | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-5357_1022-534 others(22): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391525 | |||||||
| chr13:52391742 | C | G | 2 | a0001c0002t0001g0145 a0001c0002t0001g0146 |
2 | NA18942.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1021+5490G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391742 | |||||||
| chr13:52391823 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1021+5409C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391823 | |||||||
| chr13:52391917 | G | T | 1 | a0001c0002t0001g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021+5315C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391917 | |||||||
| chr13:52391930 | T | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+5302A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391930 | |||||||
| chr13:52391959 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
6 | HG01255.hp1 HG01256.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+5273C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52391959 | |||||||
| chr13:52392020 | A | G | 29 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0045 others(26): Show |
35 | HG00544.hp2 HG01099.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1021+5212T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392020 | |||||||
| chr13:52392052 | C | T | 4 | a0002c0003t0003g0186 a0002c0003t0003g0187 a0002c0003t0003g0188 others(1): Show |
4 | HG00544.hp2 NA18994.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+5180G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392052 | |||||||
| chr13:52392055 | G | A | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+5177C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392055 | |||||||
| chr13:52392064 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+5168G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392064 | |||||||
| chr13:52392122 | A | G | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+5110T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392122 | |||||||
| chr13:52392134 | G | A | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1021+5098C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392134 | |||||||
| chr13:52392153 | C | T | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1021+5079G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392153 | |||||||
| chr13:52392156 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1021+5076G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392156 | |||||||
| chr13:52392190 | C | CA | 21 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0045 others(18): Show |
24 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1021+5041dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392190 | |||||||
| chr13:52392190 | C | CAA | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
124 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1021+5040_1021+504 others(6): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392190 | |||||||
| chr13:52392190 | C | CAAA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0092 others(10): Show |
14 | HG00438.hp2 HG00735.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+5039_1021+504 others(7): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392190 | |||||||
| chr13:52392190 | C | CAAAAAAA | 5 | a0002c0003t0003g0189 a0003c0004t0001g0014 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+5035_1021+504 others(11): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392190 | |||||||
| chr13:52392211 | AG | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+5020delC | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392211 | |||||||
| chr13:52392214 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+5018T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392214 | |||||||
| chr13:52392497 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021+4735G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392497 | |||||||
| chr13:52392516 | G | A | 1 | a0005c0005t0002g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1021+4716C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392516 | |||||||
| chr13:52392633 | T | C | 1 | a0001c0002t0001g0136 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1021+4599A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392633 | |||||||
| chr13:52392822 | A | G | 2 | a0001c0002t0001g0028 a0001c0002t0001g0073 |
3 | NA18950.hp1 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1021+4410T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392822 | |||||||
| chr13:52392874 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1021+4358G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392874 | |||||||
| chr13:52392902 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1021+4330A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392902 | |||||||
| chr13:52392931 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+4301T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392931 | |||||||
| chr13:52392938 | T | A | 1 | a0004c0006t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1021+4294A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392938 | |||||||
| chr13:52392939 | T | C | 1 | a0004c0006t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1021+4293A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392939 | |||||||
| chr13:52392994 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1021+4238G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52392994 | |||||||
| chr13:52393056 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1021+4176A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393056 | |||||||
| chr13:52393260 | T | C | 1 | a0001c0002t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1021+3972A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393260 | |||||||
| chr13:52393303 | G | A | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+3929C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393303 | |||||||
| chr13:52393307 | A | C | 1 | a0001c0002t0001g0027 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1021+3925T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393307 | |||||||
| chr13:52393487 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+3745C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393487 | |||||||
| chr13:52393519 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1021+3713T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393519 | |||||||
| chr13:52393565 | G | A | 2 | a0004c0006t0001g0173 a0004c0020t0001g0172 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1021+3667C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393565 | |||||||
| chr13:52393842 | T | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+3390A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393842 | |||||||
| chr13:52393975 | C | G | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1021+3257G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52393975 | |||||||
| chr13:52394087 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1021+3145G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394087 | |||||||
| chr13:52394096 | C | T | 2 | a0001c0009t0001g0047 a0001c0009t0001g0048 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1021+3136G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394096 | |||||||
| chr13:52394106 | G | A | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+3126C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394106 | |||||||
| chr13:52394171 | G | A | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021+3061C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394171 | |||||||
| chr13:52394205 | C | A | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+3027G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394205 | |||||||
| chr13:52394269 | T | C | 29 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0045 others(26): Show |
35 | HG00544.hp2 HG01099.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1021+2963A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394269 | |||||||
| chr13:52394281 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1021+2951C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394281 | |||||||
| chr13:52394352 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(2): Show |
6 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+2880C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394352 | |||||||
| chr13:52394416 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1021+2816G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394416 | |||||||
| chr13:52394417 | C | A | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+2815G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394417 | |||||||
| chr13:52394443 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1021+2789C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394443 | |||||||
| chr13:52394475 | A | G | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+2757T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394475 | |||||||
| chr13:52394485 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1021+2747C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394485 | |||||||
| chr13:52394510 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
143 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1021+2722T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394510 | |||||||
| chr13:52394531 | T | C | 1 | a0003c0004t0001g0014 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1021+2701A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394531 | |||||||
| chr13:52394602 | A | G | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1021+2630T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394602 | |||||||
| chr13:52394609 | C | T | 3 | a0001c0002t0001g0008 a0001c0002t0001g0059 a0001c0002t0001g0110 |
5 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021+2623G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394609 | |||||||
| chr13:52394613 | G | GA | 10 | a0001c0001t0001g0107 a0001c0001t0001g0162 a0001c0002t0001g0030 others(7): Show |
12 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+2618dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394613 | |||||||
| chr13:52394613 | GA | G | 5 | a0001c0002t0001g0026 a0005c0005t0002g0182 a0005c0005t0002g0183 others(2): Show |
6 | HG01070.hp2 HG01243.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+2618delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394613 | |||||||
| chr13:52394731 | C | T | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+2501G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394731 | |||||||
| chr13:52394935 | C | A | 1 | a0001c0002t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1021+2297G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394935 | |||||||
| chr13:52394997 | A | G | 21 | a0001c0002t0001g0008 a0001c0002t0001g0059 a0002c0003t0003g0038 others(18): Show |
27 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1021+2235T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52394997 | |||||||
| chr13:52395015 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(185): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1021+2217C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52395015 | |||||||
| chr13:52395183 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0111 |
2 | HG01074.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1021+2049G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52395183 | |||||||
| chr13:52395710 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1021+1522C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52395710 | |||||||
| chr13:52395985 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1021+1247G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52395985 | |||||||
| chr13:52396196 | T | C | 1 | a0002c0003t0003g0190 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1021+1036A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396196 | |||||||
| chr13:52396202 | CAG | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
6 | HG01255.hp1 HG01256.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+1028_1021+102 others(6): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396202 | |||||||
| chr13:52396250 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0163 |
3 | NA18974.hp1 NA18989.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1021+982C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396250 | |||||||
| chr13:52396263 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1021+969G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396263 | |||||||
| chr13:52396394 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0175 others(2): Show |
7 | HG01255.hp1 HG01256.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1021+838G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396394 | |||||||
| chr13:52396413 | T | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+819A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396413 | |||||||
| chr13:52396479 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0097 |
3 | HG00621.hp1 NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1021+753C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396479 | |||||||
| chr13:52396524 | TCAAAACA others(3): Show |
T | 1 | a0004c0006t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1021+698_1021+707d others(12): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396524 | |||||||
| chr13:52396762 | G | C | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+470C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396762 | |||||||
| chr13:52396765 | C | G | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+467G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396765 | |||||||
| chr13:52396800 | T | C | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+432A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396800 | |||||||
| chr13:52396879 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1021+353A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396879 | |||||||
| chr13:52396985 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1021+247G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 3/4 | chr13 | 52396985 | |||||||
| chr13:52398313 | G | A | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-119C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398313 | |||||||
| chr13:52398324 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0111 |
2 | HG01074.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.59-130C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398324 | |||||||
| chr13:52398395 | G | A | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-201C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398395 | |||||||
| chr13:52398570 | A | T | 2 | a0004c0006t0001g0173 a0004c0020t0001g0172 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.59-376T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398570 | |||||||
| chr13:52398787 | A | T | 2 | a0007c0013t0001g0084 a0007c0013t0001g0150 |
2 | HG02056.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.59-593T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398787 | |||||||
| chr13:52398792 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.59-598C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398792 | |||||||
| chr13:52398820 | G | T | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-626C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398820 | |||||||
| chr13:52398822 | T | G | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-628A>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398822 | |||||||
| chr13:52398823 | G | GGAATCT | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-630_59-629insAG others(4): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398823 | |||||||
| chr13:52398853 | G | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
11 | HG00408.hp1 HG00621.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-659C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52398853 | |||||||
| chr13:52399378 | AG | A | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-1185delC | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399378 | |||||||
| chr13:52399478 | C | A | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-1284G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399478 | |||||||
| chr13:52399515 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.59-1321A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399515 | |||||||
| chr13:52399543 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.59-1349T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399543 | |||||||
| chr13:52399610 | T | TTC | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1418_59-1417dup others(2): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399610 | |||||||
| chr13:52399812 | A | C | 1 | a0001c0002t0001g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.59-1618T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399812 | |||||||
| chr13:52399863 | C | A | 1 | a0001c0018t0001g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.59-1669G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399863 | |||||||
| chr13:52399874 | G | A | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1680C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399874 | |||||||
| chr13:52399951 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.59-1757T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52399951 | |||||||
| chr13:52400096 | T | A | 1 | a0001c0002t0005g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59-1902A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400096 | T | TA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(10): Show |
16 | HG01192.hp1 HG01256.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-1903dupT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400096 | T | TAA | 5 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(2): Show |
6 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1904_59-1903dup others(2): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400096 | T | TAAA | 4 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(1): Show |
6 | HG01243.hp2 HG06807.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1905_59-1903dup others(3): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400096 | TA | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0068 a0001c0001t0001g0083 others(7): Show |
12 | HG01074.hp2 HG01256.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1903delT | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400096 | TAAAA | T | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-1906_59-1903del others(4): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400096 | |||||||
| chr13:52400443 | C | G | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2100G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400443 | |||||||
| chr13:52400492 | G | A | 1 | a0001c0011t0001g0031 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.58+2051C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400492 | |||||||
| chr13:52400572 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.58+1971G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400572 | |||||||
| chr13:52400603 | A | AAAAC | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+1936_58+1939dup others(4): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400603 | |||||||
| chr13:52400682 | A | T | 19 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(16): Show |
23 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.58+1861T>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400682 | |||||||
| chr13:52400884 | G | C | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1659C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400884 | |||||||
| chr13:52400941 | T | C | 1 | a0001c0002t0001g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58+1602A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400941 | |||||||
| chr13:52400941 | TGTAGA | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(1): Show |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1597_58+1601del others(5): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400941 | |||||||
| chr13:52400945 | G | A | 1 | a0001c0002t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+1598C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52400945 | |||||||
| chr13:52401177 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0108 others(1): Show |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1366C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401177 | |||||||
| chr13:52401224 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+1319G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401224 | |||||||
| chr13:52401307 | T | C | 2 | a0001c0002t0001g0145 a0001c0002t0001g0146 |
2 | NA18942.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.58+1236A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401307 | |||||||
| chr13:52401361 | G | A | 10 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(7): Show |
12 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+1182C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401361 | |||||||
| chr13:52401445 | C | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.58+1098G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401445 | |||||||
| chr13:52401549 | C | T | 15 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(12): Show |
18 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.58+994G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401549 | |||||||
| chr13:52401567 | G | A | 6 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(3): Show |
7 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+976C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401567 | |||||||
| chr13:52401595 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.58+948C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401595 | |||||||
| chr13:52401702 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
137 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.58+841A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401702 | |||||||
| chr13:52401751 | C | T | 2 | a0003c0004t0002g0180 a0003c0004t0002g0181 |
2 | HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.58+792G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401751 | |||||||
| chr13:52401913 | T | C | 1 | a0008c0010t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.58+630A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52401913 | |||||||
| chr13:52402107 | G | A | 2 | a0001c0001t0001g0106 a0011c0019t0002g0178 |
2 | HG02970.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.58+436C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402107 | |||||||
| chr13:52402146 | T | C | 2 | a0001c0009t0001g0047 a0001c0009t0001g0048 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.58+397A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402146 | |||||||
| chr13:52402165 | G | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
179 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.58+378C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402165 | |||||||
| chr13:52402356 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.58+187C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402356 | |||||||
| chr13:52402412 | A | C | 9 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(6): Show |
11 | HG01243.hp1 HG01243.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+131T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402412 | |||||||
| chr13:52402475 | A | G | 1 | a0003c0004t0001g0014 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58+68T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402475 | |||||||
| chr13:52402508 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.58+35G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402508 | |||||||
| chr13:52402514 | G | A | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+29C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 2/4 | chr13 | 52402514 | |||||||
| chr13:52402960 | C | T | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-279G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52402960 | |||||||
| chr13:52403230 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-81-549A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403230 | |||||||
| chr13:52403333 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0060 |
5 | HG00423.hp1 HG01175.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-652G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403333 | |||||||
| chr13:52403354 | A | G | 3 | a0001c0002t0001g0008 a0001c0002t0001g0059 a0001c0002t0001g0110 |
5 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-673T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403354 | |||||||
| chr13:52403520 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-81-839G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403520 | |||||||
| chr13:52403815 | T | C | 1 | a0001c0002t0001g0166 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-81-1134A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403815 | |||||||
| chr13:52403906 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-81-1225A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403906 | |||||||
| chr13:52403928 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02083.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-81-1247G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403928 | |||||||
| chr13:52403938 | A | AT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0043 others(13): Show |
22 | HG00140.hp1 HG00423.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-81-1258dupA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | A | ATT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0054 others(4): Show |
8 | HG01106.hp1 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-1259_-81-1258d others(4): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0174 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-81-1268_-81-1258d others(13): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | AT | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0032 others(77): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-81-1258delA | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | ATT | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0169 a0001c0002t0001g0035 others(5): Show |
12 | HG01069.hp2 HG01243.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-1259_-81-1258d others(4): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | ATTTTTT | A | 9 | a0002c0003t0003g0038 a0002c0003t0003g0186 a0002c0003t0003g0187 others(6): Show |
10 | HG00544.hp2 HG01099.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-1263_-81-1258d others(8): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403938 | ATTTTTTT others(3): Show |
A | 1 | a0001c0002t0001g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-81-1267_-81-1258d others(12): Show |
THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403938 | |||||||
| chr13:52403966 | T | A | 4 | a0004c0006t0001g0037 a0004c0006t0001g0171 a0004c0006t0001g0173 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-1285A>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403966 | |||||||
| chr13:52403968 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-81-1287C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52403968 | |||||||
| chr13:52404007 | G | C | 5 | a0003c0004t0001g0014 a0003c0004t0002g0179 a0003c0004t0002g0180 others(2): Show |
7 | HG01243.hp2 HG02970.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-1326C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404007 | |||||||
| chr13:52404041 | A | G | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-81-1360T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404041 | |||||||
| chr13:52404089 | A | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-81-1408T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404089 | |||||||
| chr13:52404195 | C | T | 1 | a0011c0019t0002g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-81-1514G>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404195 | |||||||
| chr13:52404225 | C | A | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-1544G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404225 | |||||||
| chr13:52404266 | A | C | 4 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 others(1): Show |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-1585T>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404266 | |||||||
| chr13:52404312 | G | C | 4 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 others(1): Show |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-1631C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404312 | |||||||
| chr13:52404880 | T | C | 4 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 others(1): Show |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+1151A>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404880 | |||||||
| chr13:52404904 | C | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
6 | HG01255.hp1 HG01256.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82+1127G>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52404904 | |||||||
| chr13:52405040 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0009t0001g0046 others(2): Show |
6 | HG01192.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+991T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405040 | |||||||
| chr13:52405271 | A | G | 4 | a0003c0004t0002g0179 a0003c0004t0002g0180 a0003c0004t0002g0181 others(1): Show |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+760T>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405271 | |||||||
| chr13:52405535 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-82+496C>G | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405535 | |||||||
| chr13:52405660 | C | G | 1 | a0001c0002t0001g0016 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-82+371G>C | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405660 | |||||||
| chr13:52405893 | G | A | 4 | a0005c0005t0002g0182 a0005c0005t0002g0183 a0005c0005t0002g0184 others(1): Show |
4 | HG01243.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+138C>T | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405893 | |||||||
| chr13:52405933 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG01175.hp1 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-82+98C>A | THSD1 | ENSG00000136114.17 | transcript | ENST00000258613.5 | protein_coding | 1/4 | chr13 | 52405933 |