Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79866 |
| ensemblid | ENSG00000136122.18 |
| hgncid | 24724 |
| symbol | BORA |
| name | BORA aurora kinase A activator |
| refseq_nuc | NM_024808.5 |
| refseq_prot | NP_079084.4 |
| ensembl_nuc | ENST00000390667.11 |
| ensembl_prot | ENSP00000375082.6 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 72727923 |
| end | 72756196 |
| strand | + |
| ver | v1.2 |
| region | chr13:72727923-72756196 |
| region5000 | chr13:72722923-72761196 |
| regionname0 | BORA_chr13_72727923_72756196 |
| regionname5000 | BORA_chr13_72722923_72761196 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 559 | 379 | 92 | 61 | 166 | 17 | 41 | 125 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| a0002 | 0/0 | 559 | 4 | 1 | 1 | 0 | 1 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| a0003 | 0/0 | 559 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| a0004 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| a0005 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| a0006 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | MGDVK others(554): Show |
chr13 | 72722923 | 72761196 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 331 | 92 | 57 | 125 | 16 | 39 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0001c0002 | 0/0 | 1677 | 38 | 0 | 0 | 36 | 1 | 1 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0001c0003 | 0/0 | 1677 | 7 | 0 | 2 | 4 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0001c0006 | 0/0 | 1677 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0001c0007 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0002c0004 | 0/0 | 1677 | 4 | 1 | 1 | 0 | 1 | 1 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0003c0005 | 0/0 | 1677 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0004c0008 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0005c0009 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 | ||
| a0006c0010 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | ATGGG others(1672): Show |
chr13 | 72722923 | 72761196 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2784 | 224 | 69 | 32 | 80 | 11 | 31 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0002 | 1/0 | 2760 | 89 | 18 | 19 | 39 | 5 | 7 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0003 | 0/0 | 2784 | 5 | 0 | 1 | 4 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0004 | 0/0 | 2784 | 3 | 1 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0005 | 0/0 | 2784 | 3 | 2 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0006 | 0/0 | 2784 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0007 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0008 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0009 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0010 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0001c0001t0011 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0001c0002t0001 | 0/0 | 2784 | 36 | 0 | 0 | 34 | 1 | 1 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0002t0002 | 0/0 | 2760 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0001c0003t0001 | 0/0 | 2784 | 7 | 0 | 2 | 4 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0006t0001 | 0/0 | 2784 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0001c0007t0001 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0002c0004t0002 | 0/0 | 2760 | 4 | 1 | 1 | 0 | 1 | 1 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0003c0005t0001 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0004c0008t0001 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2779): Show |
chr13 | 72722923 | 72761196 |
| a0005c0009t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| a0006c0010t0002 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | AAAGA others(2755): Show |
chr13 | 72722923 | 72761196 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 0 | 7 | 11 | 1 | 6 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0003 | 0/0 | 23 | 1 | 0 | 21 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0005 | 0/0 | 10 | 6 | 1 | 2 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 3 | 3 | 1 | 3 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 2 | 0 | 3 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0002 | 0/0 | 26 | 0 | 1 | 22 | 1 | 2 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0005g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0001t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0004 | 0/0 | 20 | 0 | 0 | 18 | 1 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0003t0001g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0006t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0001c0007t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0002c0004t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0002c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0002c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0003c0005t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0004c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0005c0009t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| a0006c0010t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | FIN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00408 | hp2 | a0004 | c0008 | t0001 | g0001 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0123 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01256 | hp2 | a0001 | c0006 | t0001 | g0128 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01258 | hp1 | a0001 | c0006 | t0001 | g0129 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01258 | hp2 | a0002 | c0004 | t0002 | g0002 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02055 | hp1 | a0005 | c0009 | t0002 | g0185 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CDX | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02258 | hp1 | a0002 | c0004 | t0002 | g0002 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02895 | hp2 | a0003 | c0005 | t0001 | g0010 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02897 | hp2 | a0003 | c0005 | t0001 | g0010 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0108 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0119 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03491 | hp1 | a0002 | c0004 | t0002 | g0059 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0009 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | YRI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | CHB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18983 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19006 | hp2 | a0006 | c0010 | t0002 | g0060 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19067 | hp1 | a0001 | c0007 | t0001 | g0019 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ASW | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | TSI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20752 | hp2 | a0002 | c0004 | t0002 | g0061 | EUR | TSI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | GIH | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | USA | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | USA | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0067 | REF | REF | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0179 | REF | REF | BORA_chr13_72722923_72761196 | BORA | chr13 | 72722923 | 72761196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:72729058 | G | A | 1 | a0003 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.118G>A | p.Ala40Thr | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/12 | 218/2760 | 118/1680 | 40/559 | chr13 | 72729058 | |||
| chr13:72745098 | C | T | 1 | a0002 | 4 | HG01258.hp2 HG02258.hp1 HG03491.hp1 others(1): Show |
missense_variant | MODERATE | c.629C>T | p.Ser210Leu | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/12 | 729/2760 | 629/1680 | 210/559 | chr13 | 72745098 | |||
| chr13:72746043 | A | G | 1 | a0006 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.838A>G | p.Ile280Val | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 9/12 | 938/2760 | 838/1680 | 280/559 | chr13 | 72746043 | |||
| chr13:72746637 | G | T | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1008G>T | p.Gln336His | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/12 | 1108/2760 | 1008/1680 | 336/559 | chr13 | 72746637 | |||
| chr13:72746918 | A | G | 1 | a0004 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1289A>G | p.Asn430Ser | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/12 | 1389/2760 | 1289/1680 | 430/559 | chr13 | 72746918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:72745033 | T | C | 2 | a0001c0002 a0001c0007 |
39 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
synonymous_variant | LOW | c.564T>C | p.Ser188Ser | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/12 | 664/2760 | 564/1680 | 188/559 | chr13 | 72745033 | |||
| chr13:72746589 | T | C | 1 | a0001c0007 | 1 | NA19067.hp1 | synonymous_variant | LOW | c.960T>C | p.Tyr320Tyr | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/12 | 1060/2760 | 960/1680 | 320/559 | chr13 | 72746589 | |||
| chr13:72746718 | A | G | 1 | a0001c0006 | 2 | HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.1089A>G | p.Glu363Glu | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/12 | 1189/2760 | 1089/1680 | 363/559 | chr13 | 72746718 | |||
| chr13:72746754 | A | C | 1 | a0001c0003 | 7 | HG01192.hp2 HG01981.hp1 HG02074.hp1 others(4): Show |
synonymous_variant | LOW | c.1125A>C | p.Ser375Ser | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/12 | 1225/2760 | 1125/1680 | 375/559 | chr13 | 72746754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:72755219 | T | C | 1 | a0001c0001t0007 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 3 | chr13 | 72755219 | ||||||
| chr13:72755220 | G | A | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*4G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 4 | chr13 | 72755220 | ||||||
| chr13:72755259 | G | A | 1 | a0001c0001t0010 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 43 | chr13 | 72755259 | ||||||
| chr13:72755261 | A | G | 1 | a0001c0001t0005 | 3 | HG00735.hp1 HG02572.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*45A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 45 | chr13 | 72755261 | ||||||
| chr13:72755351 | A | C | 1 | a0001c0001t0003 | 5 | HG01243.hp2 NA18939.hp2 NA18964.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 135 | chr13 | 72755351 | ||||||
| chr13:72755490 | A | T | 1 | a0001c0001t0006 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 274 | chr13 | 72755490 | ||||||
| chr13:72755514 | T | G | 1 | a0001c0001t0004 | 3 | HG01069.hp1 HG01071.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*298T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 298 | chr13 | 72755514 | ||||||
| chr13:72755764 | A | G | 1 | a0001c0001t0011 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 548 | chr13 | 72755764 | ||||||
| chr13:72755884 | A | G | 1 | a0001c0001t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 668 | chr13 | 72755884 | ||||||
| chr13:72756163 | T | C | 1 | a0001c0001t0008 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*947T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 947 | chr13 | 72756163 | ||||||
| chr13:72756175 | G | GAATAATT others(17): Show |
14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*964_*965insTTCATA others(18): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 12/12 | 965 | INFO_REALIGN_3_PRIME | chr13 | 72756175 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:72728019 | CT | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-16+15delT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 72728019 | ||||||
| chr13:72728042 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-16+35C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728042 | |||||||
| chr13:72728089 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-16+82C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728089 | |||||||
| chr13:72728123 | G | A | 31 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0028 others(28): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-16+116G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728123 | |||||||
| chr13:72728188 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0008g0009 |
7 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+181G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728188 | |||||||
| chr13:72728240 | T | C | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-16+233T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728240 | |||||||
| chr13:72728343 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(159): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-16+336G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728343 | |||||||
| chr13:72728553 | T | A | 1 | a0001c0001t0002g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15-373T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728553 | |||||||
| chr13:72728554 | A | T | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-15-372A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728554 | |||||||
| chr13:72728568 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-15-358C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728568 | |||||||
| chr13:72728709 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15-217T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728709 | |||||||
| chr13:72728835 | G | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-91G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 1/11 | chr13 | 72728835 | |||||||
| chr13:72729208 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153+115A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729208 | |||||||
| chr13:72729284 | AT | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.153+204delT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 72729284 | ||||||
| chr13:72729454 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.153+361G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729454 | |||||||
| chr13:72729617 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.153+524A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729617 | |||||||
| chr13:72729778 | CAAAAT | C | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+688_153+692del others(5): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 72729778 | ||||||
| chr13:72729884 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.153+791T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729884 | |||||||
| chr13:72729892 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.153+799A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729892 | |||||||
| chr13:72729899 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.153+806A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72729899 | |||||||
| chr13:72730091 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0182 |
3 | HG02280.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.153+998G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730091 | |||||||
| chr13:72730094 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.153+1001C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730094 | |||||||
| chr13:72730344 | A | C | 1 | a0001c0001t0002g0155 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.154-937A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730344 | |||||||
| chr13:72730345 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.154-936T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730345 | |||||||
| chr13:72730379 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.154-902G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730379 | |||||||
| chr13:72730721 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-560C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730721 | |||||||
| chr13:72730722 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-559G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730722 | |||||||
| chr13:72730888 | T | TA | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01123.hp2 HG01981.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-371dupA | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 72730888 | ||||||
| chr13:72730889 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154-392A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730889 | |||||||
| chr13:72730898 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.154-383A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730898 | |||||||
| chr13:72730900 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-381A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730900 | |||||||
| chr13:72730902 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154-379A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730902 | |||||||
| chr13:72730906 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(84): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.154-375A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730906 | |||||||
| chr13:72730907 | A | C | 3 | a0001c0001t0005g0037 a0001c0002t0001g0038 a0001c0002t0002g0116 |
5 | HG00735.hp1 NA18522.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-374A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730907 | |||||||
| chr13:72730910 | AT | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.154-370delT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730910 | |||||||
| chr13:72730911 | T | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(37): Show |
71 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.154-370T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730911 | |||||||
| chr13:72730939 | G | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0020 others(5): Show |
11 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-342G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730939 | |||||||
| chr13:72730991 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.154-290C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730991 | |||||||
| chr13:72730998 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-283G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72730998 | |||||||
| chr13:72731018 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.154-263A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72731018 | |||||||
| chr13:72731029 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(163): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.154-252G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72731029 | |||||||
| chr13:72731073 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0002g0183 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.154-208A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72731073 | |||||||
| chr13:72731107 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.154-174G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 2/11 | chr13 | 72731107 | |||||||
| chr13:72731531 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.260+144G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72731531 | |||||||
| chr13:72731533 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260+146T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72731533 | |||||||
| chr13:72731660 | TAAGAG | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(63): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.260+278_260+282del others(5): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 72731660 | ||||||
| chr13:72731850 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260+463A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72731850 | |||||||
| chr13:72731878 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.260+491C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72731878 | |||||||
| chr13:72732021 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.260+634C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732021 | |||||||
| chr13:72732068 | G | C | 1 | a0001c0002t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.260+681G>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732068 | |||||||
| chr13:72732224 | A | G | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.260+837A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732224 | |||||||
| chr13:72732294 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.260+907A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732294 | |||||||
| chr13:72732446 | G | A | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260+1059G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732446 | |||||||
| chr13:72732466 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0152 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.260+1079T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732466 | |||||||
| chr13:72732569 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0182 |
3 | HG02280.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.260+1182C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732569 | |||||||
| chr13:72732577 | C | T | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260+1190C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732577 | |||||||
| chr13:72732819 | C | G | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260+1432C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732819 | |||||||
| chr13:72732923 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0065 |
5 | HG02155.hp2 NA18975.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+1536A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732923 | |||||||
| chr13:72732998 | T | G | 1 | a0001c0001t0002g0011 | 4 | HG00408.hp1 HG00597.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+1611T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72732998 | |||||||
| chr13:72733229 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0090 others(1): Show |
6 | HG00609.hp2 HG02040.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-1731C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733229 | |||||||
| chr13:72733233 | A | T | 1 | a0001c0001t0002g0036 | 2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.261-1727A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733233 | |||||||
| chr13:72733361 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.261-1599G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733361 | |||||||
| chr13:72733389 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.261-1571A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733389 | |||||||
| chr13:72733825 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0182 |
3 | HG02280.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.261-1135T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733825 | |||||||
| chr13:72733859 | T | C | 1 | a0001c0003t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.261-1101T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733859 | |||||||
| chr13:72733892 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0006g0029 a0001c0001t0008g0009 |
9 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.261-1068C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733892 | |||||||
| chr13:72733929 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0002g0183 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.261-1031A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72733929 | |||||||
| chr13:72734052 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0002g0183 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.261-908G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734052 | |||||||
| chr13:72734294 | T | TAAATAAA | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-666_261-665ins others(7): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734294 | |||||||
| chr13:72734295 | G | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-665G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734295 | |||||||
| chr13:72734296 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
7 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-664G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734296 | |||||||
| chr13:72734484 | G | T | 6 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.261-476G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734484 | |||||||
| chr13:72734726 | T | C | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.261-234T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734726 | |||||||
| chr13:72734763 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.261-197C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734763 | |||||||
| chr13:72734781 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.261-179C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734781 | |||||||
| chr13:72734891 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.261-69G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734891 | |||||||
| chr13:72734893 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.261-67T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734893 | |||||||
| chr13:72734929 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0089 |
3 | HG00323.hp2 HG02602.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.261-31A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 3/11 | chr13 | 72734929 | |||||||
| chr13:72735081 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.306+76T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735081 | |||||||
| chr13:72735089 | A | G | 1 | a0001c0001t0003g0143 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.306+84A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735089 | |||||||
| chr13:72735093 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.306+88C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735093 | |||||||
| chr13:72735140 | T | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(23): Show |
61 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.306+135T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735140 | |||||||
| chr13:72735209 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(159): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.306+204C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735209 | |||||||
| chr13:72735224 | A | G | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+219A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735224 | |||||||
| chr13:72735252 | G | A | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.306+247G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735252 | |||||||
| chr13:72735490 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(33): Show |
50 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.306+485G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735490 | |||||||
| chr13:72735511 | A | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG02976.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.306+506A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735511 | |||||||
| chr13:72735556 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.306+551T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735556 | |||||||
| chr13:72735592 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.306+587A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735592 | |||||||
| chr13:72735622 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(33): Show |
50 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.306+617T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735622 | |||||||
| chr13:72735748 | TACAGGCA others(6): Show |
T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.306+746_306+758del others(13): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 72735748 | ||||||
| chr13:72735766 | C | G | 1 | a0001c0001t0001g0032 | 2 | HG00323.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+761C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735766 | |||||||
| chr13:72735797 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.306+792C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735797 | |||||||
| chr13:72735802 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0167 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.306+797T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735802 | |||||||
| chr13:72735900 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.306+895C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735900 | |||||||
| chr13:72735908 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18983.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.306+903C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72735908 | |||||||
| chr13:72736129 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.306+1124C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736129 | |||||||
| chr13:72736137 | C | T | 5 | a0001c0001t0002g0036 a0001c0001t0002g0088 a0001c0001t0002g0094 others(2): Show |
6 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+1132C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736137 | |||||||
| chr13:72736270 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.306+1265T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736270 | |||||||
| chr13:72736299 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0011g0119 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.306+1294T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736299 | |||||||
| chr13:72736449 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18983.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.306+1444C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736449 | |||||||
| chr13:72736477 | A | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0118 others(28): Show |
59 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.306+1472A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736477 | |||||||
| chr13:72736500 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0168 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.307-1462T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736500 | |||||||
| chr13:72736588 | C | A | 1 | a0001c0001t0002g0041 | 2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.307-1374C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736588 | |||||||
| chr13:72736689 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.307-1273C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736689 | |||||||
| chr13:72736733 | T | C | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-1229T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736733 | |||||||
| chr13:72736870 | C | CT | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(49): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.307-1081dupT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 72736870 | ||||||
| chr13:72736870 | CT | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(71): Show |
154 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.307-1081delT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 72736870 | ||||||
| chr13:72736874 | T | G | 1 | a0001c0001t0002g0039 | 2 | HG01123.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.307-1088T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736874 | |||||||
| chr13:72736915 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.307-1047A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72736915 | |||||||
| chr13:72736983 | T | TA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0153 others(4): Show |
9 | HG02970.hp1 HG02970.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-962dupA | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 72736983 | ||||||
| chr13:72736983 | TA | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0077 others(12): Show |
20 | HG01070.hp1 HG01071.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.307-962delA | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 72736983 | ||||||
| chr13:72737127 | G | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.307-835G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72737127 | |||||||
| chr13:72737351 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0008g0009 |
8 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.307-611T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72737351 | |||||||
| chr13:72737742 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(58): Show |
136 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.307-220G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 4/11 | chr13 | 72737742 | |||||||
| chr13:72738221 | G | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.388+178G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738221 | |||||||
| chr13:72738261 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.388+218T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738261 | |||||||
| chr13:72738557 | C | T | 1 | a0001c0001t0004g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.388+514C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738557 | |||||||
| chr13:72738691 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0160 |
3 | HG01891.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.388+648C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738691 | |||||||
| chr13:72738803 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0008g0009 |
8 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+760G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738803 | |||||||
| chr13:72738823 | T | C | 3 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0063 |
3 | HG01175.hp1 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.388+780T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738823 | |||||||
| chr13:72738999 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(61): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.388+956G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72738999 | |||||||
| chr13:72739036 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388+993A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739036 | |||||||
| chr13:72739113 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.388+1070A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739113 | |||||||
| chr13:72739262 | A | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0054 others(31): Show |
82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.388+1219A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739262 | |||||||
| chr13:72739310 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.388+1267G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739310 | |||||||
| chr13:72739350 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.388+1307T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739350 | |||||||
| chr13:72739380 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0006g0029 others(1): Show |
10 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1337G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739380 | |||||||
| chr13:72739426 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.388+1383G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739426 | |||||||
| chr13:72739459 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.388+1416C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739459 | |||||||
| chr13:72739580 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0002g0012 |
5 | HG01175.hp2 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+1537G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739580 | |||||||
| chr13:72739592 | T | C | 12 | a0001c0002t0001g0004 a0001c0002t0001g0019 a0001c0002t0001g0031 others(9): Show |
33 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.388+1549T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739592 | |||||||
| chr13:72739672 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.388+1629T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739672 | |||||||
| chr13:72739687 | G | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(78): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.388+1644G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739687 | |||||||
| chr13:72739697 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388+1654C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739697 | |||||||
| chr13:72739742 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0094 a0001c0001t0002g0114 |
3 | HG01099.hp1 HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.388+1699A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739742 | |||||||
| chr13:72739822 | T | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(47): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.388+1779T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739822 | |||||||
| chr13:72739875 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0054 others(31): Show |
82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.388+1832G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739875 | |||||||
| chr13:72739990 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0167 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.388+1947C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72739990 | |||||||
| chr13:72740018 | T | TG | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(38): Show |
61 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.388+1981dupG | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72740018 | ||||||
| chr13:72740018 | TG | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
319 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.388+1981delG | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72740018 | ||||||
| chr13:72740032 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.388+1989G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740032 | |||||||
| chr13:72740070 | C | T | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.388+2027C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740070 | |||||||
| chr13:72740138 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0152 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.388+2095C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740138 | |||||||
| chr13:72740297 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.388+2254A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740297 | |||||||
| chr13:72740350 | A | G | 1 | a0001c0001t0002g0011 | 4 | HG00408.hp1 HG00597.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+2307A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740350 | |||||||
| chr13:72740381 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.388+2338C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740381 | |||||||
| chr13:72740450 | T | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388+2407T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740450 | |||||||
| chr13:72740452 | A | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388+2409A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740452 | |||||||
| chr13:72740546 | T | C | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.388+2503T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740546 | |||||||
| chr13:72740548 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.388+2505C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740548 | |||||||
| chr13:72740575 | G | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.388+2532G>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740575 | |||||||
| chr13:72740687 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.388+2644T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740687 | |||||||
| chr13:72740760 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388+2717A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740760 | |||||||
| chr13:72740762 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388+2719A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740762 | |||||||
| chr13:72740799 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.389-2738G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740799 | |||||||
| chr13:72740906 | T | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0056 others(1): Show |
6 | HG01192.hp1 HG01496.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-2631T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72740906 | |||||||
| chr13:72741030 | T | C | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389-2507T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741030 | |||||||
| chr13:72741072 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0156 a0001c0001t0001g0191 others(1): Show |
5 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-2465A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741072 | |||||||
| chr13:72741084 | A | G | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389-2453A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741084 | |||||||
| chr13:72741115 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.389-2422T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741115 | |||||||
| chr13:72741128 | G | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(79): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.389-2409G>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741128 | |||||||
| chr13:72741134 | G | C | 1 | a0001c0001t0002g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.389-2403G>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741134 | |||||||
| chr13:72741247 | A | G | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0156 others(3): Show |
8 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.389-2290A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741247 | |||||||
| chr13:72741624 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.389-1913A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741624 | |||||||
| chr13:72741888 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.389-1649T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741888 | |||||||
| chr13:72741941 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.389-1596G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72741941 | |||||||
| chr13:72742003 | C | G | 9 | a0001c0001t0001g0118 a0001c0001t0002g0020 a0001c0001t0002g0039 others(6): Show |
12 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.389-1534C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742003 | |||||||
| chr13:72742119 | G | A | 1 | a0001c0001t0005g0037 | 2 | HG00735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.389-1418G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742119 | |||||||
| chr13:72742289 | C | A | 1 | a0001c0001t0002g0025 | 2 | HG01496.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.389-1248C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742289 | |||||||
| chr13:72742371 | T | TAA | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0008g0009 |
8 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.389-1163_389-1162d others(4): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742371 | ||||||
| chr13:72742520 | C | A | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.389-1017C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742520 | |||||||
| chr13:72742757 | T | C | 2 | a0001c0002t0001g0038 a0001c0002t0001g0140 |
3 | NA18961.hp1 NA18968.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.389-780T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742757 | |||||||
| chr13:72742763 | TATATACA others(3): Show |
T | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.389-772_389-763del others(10): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742763 | ||||||
| chr13:72742763 | TATATACA others(13): Show |
T | 1 | a0001c0002t0001g0111 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.389-772_389-753del others(20): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742763 | ||||||
| chr13:72742765 | TATACAC | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0151 a0001c0001t0001g0178 others(2): Show |
7 | HG01952.hp2 HG01975.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-770_389-765del others(6): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(3): Show |
T | 3 | a0001c0001t0001g0136 a0001c0001t0002g0051 a0001c0001t0003g0014 |
3 | HG00741.hp1 NA18964.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.389-770_389-761del others(10): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(5): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.389-770_389-759del others(12): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(7): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.389-770_389-757del others(14): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(9): Show |
T | 2 | a0001c0002t0001g0038 a0001c0002t0001g0140 |
3 | NA18961.hp1 NA18968.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.389-770_389-755del others(16): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(11): Show |
T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0163 others(3): Show |
7 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-770_389-753del others(18): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(13): Show |
T | 12 | a0001c0001t0001g0191 a0001c0002t0001g0004 a0001c0002t0001g0019 others(9): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.389-770_389-751del others(20): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742765 | TATACACA others(17): Show |
T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0144 a0001c0001t0001g0160 others(1): Show |
5 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-770_389-747del others(24): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742765 | ||||||
| chr13:72742767 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.389-770T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742767 | |||||||
| chr13:72742767 | TACACACA others(1): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(13): Show |
29 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.389-732_389-725del others(8): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(3): Show |
T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.389-734_389-725del others(10): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(5): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0138 others(6): Show |
17 | HG00558.hp1 HG01258.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.389-736_389-725del others(12): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(7): Show |
T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0101 others(2): Show |
11 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.389-738_389-725del others(14): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(9): Show |
T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0158 a0001c0001t0001g0169 |
5 | HG02970.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-740_389-725del others(16): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(11): Show |
T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0040 others(23): Show |
37 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.389-742_389-725del others(18): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742767 | TACACACA others(13): Show |
T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0118 a0001c0001t0001g0156 others(5): Show |
9 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.389-744_389-725del others(20): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742767 | ||||||
| chr13:72742769 | C | T | 1 | a0001c0001t0002g0002 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.389-768C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742769 | |||||||
| chr13:72742777 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0092 a0001c0001t0001g0102 others(4): Show |
11 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-760C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742777 | |||||||
| chr13:72742779 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(40): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.389-758C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742779 | |||||||
| chr13:72742781 | C | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0064 a0002c0004t0002g0002 others(2): Show |
6 | HG00558.hp1 HG01258.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.389-756C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742781 | |||||||
| chr13:72742783 | C | T | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.389-754C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742783 | |||||||
| chr13:72742785 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0078 others(1): Show |
6 | HG00438.hp1 HG01074.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-752C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742785 | |||||||
| chr13:72742789 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0156 a0001c0001t0001g0176 others(2): Show |
6 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-748C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742789 | |||||||
| chr13:72742801 | CACACACA others(5): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.389-734_389-723del others(12): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742801 | ||||||
| chr13:72742803 | CACACACA others(2): Show |
C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0002g0002 others(1): Show |
4 | HG01192.hp2 NA18987.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-732_389-724del others(9): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 72742803 | ||||||
| chr13:72742868 | T | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.389-669T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742868 | |||||||
| chr13:72742966 | G | A | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.389-571G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742966 | |||||||
| chr13:72742999 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389-538C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72742999 | |||||||
| chr13:72743067 | G | A | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.389-470G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743067 | |||||||
| chr13:72743113 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.389-424T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743113 | |||||||
| chr13:72743128 | A | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
52 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.389-409A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743128 | |||||||
| chr13:72743345 | AGTTTTAT others(6): Show |
A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0008g0009 |
8 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.389-191_389-179del others(13): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743345 | |||||||
| chr13:72743360 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18987.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.389-177T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743360 | |||||||
| chr13:72743409 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.389-128T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743409 | |||||||
| chr13:72743447 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(61): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.389-90C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 5/11 | chr13 | 72743447 | |||||||
| chr13:72743602 | G | GGTGA | 39 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
54 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(51): Show |
splice_region_variant&intron_variant | LOW | c.454+3_454+6dupGAGT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 72743602 | ||||||
| chr13:72743625 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.454+23A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72743625 | |||||||
| chr13:72743709 | C | CT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(59): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.454+120dupT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 72743709 | ||||||
| chr13:72743722 | T | A | 1 | a0001c0001t0002g0086 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.454+120T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72743722 | |||||||
| chr13:72743848 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.454+246A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72743848 | |||||||
| chr13:72743851 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.454+249G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72743851 | |||||||
| chr13:72744004 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0152 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.454+402T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72744004 | |||||||
| chr13:72744062 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.455-443A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72744062 | |||||||
| chr13:72744130 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.455-375A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 6/11 | chr13 | 72744130 | |||||||
| chr13:72745344 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.738+137G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/11 | chr13 | 72745344 | |||||||
| chr13:72745391 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.738+184A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/11 | chr13 | 72745391 | |||||||
| chr13:72745772 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(61): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.739-172G>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/11 | chr13 | 72745772 | |||||||
| chr13:72745869 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.739-75A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/11 | chr13 | 72745869 | |||||||
| chr13:72745924 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.739-20A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 8/11 | chr13 | 72745924 | |||||||
| chr13:72746101 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.871+25G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 9/11 | chr13 | 72746101 | |||||||
| chr13:72746232 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.871+156C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 9/11 | chr13 | 72746232 | |||||||
| chr13:72746317 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(76): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.872-184C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 9/11 | chr13 | 72746317 | |||||||
| chr13:72747211 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1482+100G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747211 | |||||||
| chr13:72747378 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1482+267G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747378 | |||||||
| chr13:72747383 | C | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
5 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482+272C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747383 | |||||||
| chr13:72747385 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1482+274A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747385 | |||||||
| chr13:72747540 | G | T | 1 | a0001c0001t0002g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1482+429G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747540 | |||||||
| chr13:72747541 | G | GT | 6 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0001g0191 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+440dupT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72747541 | ||||||
| chr13:72747814 | T | C | 1 | a0001c0002t0001g0083 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1482+703T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747814 | |||||||
| chr13:72747824 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0040 others(25): Show |
40 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1482+713C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72747824 | |||||||
| chr13:72748097 | C | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(46): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1482+986C>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72748097 | |||||||
| chr13:72748232 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0008g0009 |
8 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1482+1121G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72748232 | |||||||
| chr13:72748372 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1482+1261C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72748372 | |||||||
| chr13:72748445 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(31): Show |
48 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.1482+1334T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72748445 | |||||||
| chr13:72748728 | T | TTC | 3 | a0001c0001t0001g0045 a0001c0001t0001g0156 a0001c0001t0001g0188 |
4 | HG02280.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+1647_1482+164 others(6): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748728 | ||||||
| chr13:72748728 | TTCTCTCT others(3): Show |
T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1482+1639_1482+164 others(14): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748728 | ||||||
| chr13:72748728 | TTCTCTCT others(7): Show |
T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(46): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1482+1635_1482+164 others(18): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748728 | ||||||
| chr13:72748728 | TTCTCTCT others(11): Show |
T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0152 a0001c0001t0009g0108 |
3 | HG02965.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1482+1631_1482+164 others(22): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748728 | ||||||
| chr13:72748742 | CTCTCTCT others(11): Show |
C | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1482+1633_1482+165 others(22): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748742 | ||||||
| chr13:72748746 | CTCTCTCT others(7): Show |
C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(58): Show |
136 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1482+1637_1482+165 others(18): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72748746 | ||||||
| chr13:72749081 | TTAGCTTT others(4): Show |
T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
190 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1482+1981_1482+199 others(15): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72749081 | ||||||
| chr13:72749362 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1482+2251A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749362 | |||||||
| chr13:72749508 | CT | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1482+2408delT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72749508 | ||||||
| chr13:72749519 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1482+2408T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749519 | |||||||
| chr13:72749539 | T | C | 9 | a0001c0001t0001g0118 a0001c0001t0002g0020 a0001c0001t0002g0039 others(6): Show |
12 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482+2428T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749539 | |||||||
| chr13:72749654 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0006g0029 others(1): Show |
10 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1482+2543T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749654 | |||||||
| chr13:72749686 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0005g0148 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1482+2575T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749686 | |||||||
| chr13:72749732 | G | A | 2 | a0001c0006t0001g0128 a0001c0006t0001g0129 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1482+2621G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749732 | |||||||
| chr13:72749835 | T | C | 1 | a0001c0001t0001g0042 | 2 | NA18961.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1482+2724T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749835 | |||||||
| chr13:72749983 | C | A | 1 | a0002c0004t0002g0059 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1482+2872C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749983 | |||||||
| chr13:72749990 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1482+2879C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749990 | |||||||
| chr13:72749997 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0158 |
4 | HG02970.hp2 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+2886G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72749997 | |||||||
| chr13:72750039 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1482+2928G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750039 | |||||||
| chr13:72750082 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0098 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1482+2971C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750082 | |||||||
| chr13:72750108 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1482+2997G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750108 | |||||||
| chr13:72750115 | T | C | 6 | a0001c0001t0001g0176 a0001c0001t0001g0182 a0001c0001t0001g0184 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482+3004T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750115 | |||||||
| chr13:72750249 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1482+3138A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750249 | |||||||
| chr13:72750470 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0002g0183 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1483-3220G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750470 | |||||||
| chr13:72750473 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1483-3217T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750473 | |||||||
| chr13:72750554 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1483-3136G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750554 | |||||||
| chr13:72750581 | T | C | 1 | a0001c0001t0005g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1483-3109T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750581 | |||||||
| chr13:72750613 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(76): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1483-3077C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750613 | |||||||
| chr13:72750759 | C | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0151 others(19): Show |
47 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1483-2931C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750759 | |||||||
| chr13:72750789 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0062 |
3 | NA18943.hp1 NA18963.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1483-2901G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750789 | |||||||
| chr13:72750835 | C | T | 1 | a0001c0001t0005g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1483-2855C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750835 | |||||||
| chr13:72750870 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1483-2820G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750870 | |||||||
| chr13:72750878 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1483-2812G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750878 | |||||||
| chr13:72750952 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1483-2738G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750952 | |||||||
| chr13:72750957 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1483-2733C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750957 | |||||||
| chr13:72750972 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1483-2718C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72750972 | |||||||
| chr13:72751004 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(61): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1483-2686A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751004 | |||||||
| chr13:72751092 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(31): Show |
48 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.1483-2598A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751092 | |||||||
| chr13:72751142 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0147 a0001c0001t0001g0187 |
4 | HG03195.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2548A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751142 | |||||||
| chr13:72751166 | A | G | 1 | a0001c0003t0001g0130 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1483-2524A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751166 | |||||||
| chr13:72751255 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1483-2435A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751255 | |||||||
| chr13:72751409 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1483-2281C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751409 | |||||||
| chr13:72751513 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0159 a0005c0009t0002g0185 |
3 | HG02055.hp1 HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1483-2177T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751513 | |||||||
| chr13:72751556 | G | GAGTATAG others(13): Show |
1 | a0001c0001t0001g0070 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1483-2129_1483-211 others(24): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72751556 | ||||||
| chr13:72751970 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1483-1720G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72751970 | |||||||
| chr13:72752093 | T | G | 1 | a0001c0001t0002g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1483-1597T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752093 | |||||||
| chr13:72752105 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1483-1585A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752105 | |||||||
| chr13:72752144 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0101 others(2): Show |
11 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483-1546T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752144 | |||||||
| chr13:72752183 | C | A | 1 | a0006c0010t0002g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1483-1507C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752183 | |||||||
| chr13:72752378 | A | AT | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0159 |
3 | HG00741.hp1 HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1483-1311dupT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72752378 | ||||||
| chr13:72752561 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1483-1129A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752561 | |||||||
| chr13:72752725 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1483-965A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752725 | |||||||
| chr13:72752777 | TAA | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1483-911_1483-910d others(4): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 72752777 | ||||||
| chr13:72752806 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1483-884A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752806 | |||||||
| chr13:72752868 | G | T | 1 | a0001c0002t0001g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1483-822G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72752868 | |||||||
| chr13:72753568 | G | A | 1 | a0005c0009t0002g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1483-122G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72753568 | |||||||
| chr13:72753573 | A | C | 1 | a0002c0004t0002g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1483-117A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72753573 | |||||||
| chr13:72753685 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | splice_region_variant&intron_variant | LOW | c.1483-5G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 10/11 | chr13 | 72753685 | |||||||
| chr13:72753868 | TATAAA | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0156 |
3 | HG02280.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1614+52_1614+56del others(5): Show |
BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr13 | 72753868 | ||||||
| chr13:72753994 | A | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0152 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1614+173A>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72753994 | |||||||
| chr13:72754067 | G | T | 1 | a0001c0001t0006g0029 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1614+246G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754067 | |||||||
| chr13:72754083 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1614+262C>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754083 | |||||||
| chr13:72754314 | C | CT | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0043 others(34): Show |
74 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1614+508dupT | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr13 | 72754314 | ||||||
| chr13:72754395 | T | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(152): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1614+574T>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754395 | |||||||
| chr13:72754489 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1615-662T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754489 | |||||||
| chr13:72754570 | T | C | 2 | a0001c0001t0005g0037 a0001c0001t0005g0148 |
3 | HG00735.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-581T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754570 | |||||||
| chr13:72754607 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1615-544A>G | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754607 | |||||||
| chr13:72754695 | A | C | 1 | a0001c0001t0001g0042 | 2 | NA18961.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1615-456A>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754695 | |||||||
| chr13:72754709 | T | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0161 |
2 | HG00438.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1615-442T>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754709 | |||||||
| chr13:72754894 | G | T | 5 | a0001c0001t0003g0014 a0001c0001t0003g0143 a0001c0001t0004g0124 others(2): Show |
9 | HG00735.hp1 HG01243.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-257G>T | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754894 | |||||||
| chr13:72754948 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1615-203G>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72754948 | |||||||
| chr13:72755113 | C | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0148 |
3 | HG00735.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-38C>A | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72755113 | |||||||
| chr13:72755120 | T | C | 2 | a0001c0001t0005g0037 a0001c0001t0005g0148 |
3 | HG00735.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-31T>C | BORA | ENSG00000136122.18 | transcript | ENST00000390667.11 | protein_coding | 11/11 | chr13 | 72755120 |