Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2155 |
| ensemblid | ENSG00000057593.14 |
| hgncid | 3544 |
| symbol | F7 |
| name | coagulation factor VII |
| refseq_nuc | NM_019616.4 |
| refseq_prot | NP_062562.1 |
| ensembl_nuc | ENST00000346342.8 |
| ensembl_prot | ENSP00000329546.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113105791 |
| end | 113120685 |
| strand | + |
| ver | v1.2 |
| region | chr13:113105791-113120685 |
| region5000 | chr13:113100791-113125685 |
| regionname0 | F7_chr13_113105791_113120685 |
| regionname5000 | F7_chr13_113100791_113125685 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 444 | 359 | 70 | 71 | 166 | 18 | 32 | 119 | F7_chr13_113100791_113125685 | F7 | MVSQA others(439): Show |
chr13 | 113100791 | 113125685 |
| a0002 | 0/0 | 444 | 37 | 12 | 4 | 7 | 0 | 14 | 6 | F7_chr13_113100791_113125685 | F7 | MVSQA others(439): Show |
chr13 | 113100791 | 113125685 |
| a0003 | 0/0 | 253 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | MVSQA others(248): Show |
chr13 | 113100791 | 113125685 |
| a0004 | 0/0 | 444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | MVSQA others(439): Show |
chr13 | 113100791 | 113125685 |
| a0005 | 0/0 | 444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | MVSQA others(439): Show |
chr13 | 113100791 | 113125685 |
| a0006 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | MVSQA others(439): Show |
chr13 | 113100791 | 113125685 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1332 | 351 | 66 | 70 | 165 | 16 | 32 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0001c0003 | 0/0 | 1332 | 6 | 4 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0001c0004 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0001c0009 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0002c0002 | 0/0 | 1332 | 35 | 12 | 3 | 6 | 0 | 14 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0002c0007 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0002c0010 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0003c0008 | 0/0 | 1321 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1316): Show |
chr13 | 113100791 | 113125685 | ||
| a0004c0005 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0005c0006 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 | ||
| a0006c0011 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | ATGGT others(1327): Show |
chr13 | 113100791 | 113125685 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3063 | 289 | 46 | 58 | 142 | 12 | 30 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0002 | 0/0 | 3063 | 28 | 0 | 9 | 19 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0004 | 0/0 | 3065 | 8 | 7 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0005 | 0/0 | 3065 | 5 | 5 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0006 | 0/1 | 3059 | 5 | 0 | 1 | 0 | 2 | 1 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3054): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0007 | 0/0 | 3063 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0012 | 0/0 | 3065 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0013 | 0/0 | 3063 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0016 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0017 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0018 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0019 | 0/0 | 3047 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3042): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0020 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3046): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0022 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0023 | 0/0 | 3059 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3054): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0024 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0001t0025 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0003t0001 | 0/0 | 3063 | 2 | 0 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0003t0010 | 0/0 | 3065 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0001c0003t0014 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0004t0001 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0001c0009t0001 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0003 | 0/0 | 3065 | 28 | 10 | 3 | 6 | 0 | 9 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0008 | 0/0 | 3065 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0009 | 0/0 | 3061 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3056): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0011 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0002c0002t0021 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0002c0007t0011 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0002c0010t0015 | 0/0 | 3065 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3060): Show |
chr13 | 113100791 | 113125685 |
| a0003c0008t0002 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3047): Show |
chr13 | 113100791 | 113125685 |
| a0004c0005t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0005c0006t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| a0006c0011t0001 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | AGTCC others(3058): Show |
chr13 | 113100791 | 113125685 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 3 | 12 | 3 | 3 | 7 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0002 | 0/0 | 11 | 6 | 3 | 0 | 1 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0003 | 0/0 | 25 | 0 | 7 | 15 | 1 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0004 | 0/0 | 25 | 1 | 5 | 14 | 2 | 3 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 3 | 8 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0007 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0002 | 0/0 | 16 | 0 | 7 | 9 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0005g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0006g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0007g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0013g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0016g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0018g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0020g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0023g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0001t0025g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0003t0010g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0003t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0003t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0001c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0008g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0008g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0009g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0002t0021g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0007t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0002c0010t0015g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0003c0008t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0004c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0005c0006t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| a0006c0011t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0029 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0029 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00609 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00673 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0038 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0161 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01496 | hp2 | a0002 | c0010 | t0015 | g0084 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0051 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0054 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0058 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01975 | hp1 | a0003 | c0008 | t0002 | g0133 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01981 | hp1 | a0001 | c0001 | t0020 | g0011 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02135 | hp1 | a0001 | c0001 | t0025 | g0034 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0057 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0063 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0055 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02602 | hp1 | a0002 | c0002 | t0021 | g0012 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02630 | hp1 | a0001 | c0003 | t0010 | g0042 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02698 | hp2 | a0001 | c0001 | t0023 | g0164 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02723 | hp2 | a0001 | c0003 | t0010 | g0042 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0068 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0066 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02809 | hp1 | a0004 | c0005 | t0001 | g0141 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0177 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0163 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0200 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03209 | hp2 | a0001 | c0003 | t0014 | g0077 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03453 | hp2 | a0005 | c0006 | t0001 | g0003 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03491 | hp2 | a0002 | c0002 | t0009 | g0023 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03492 | hp2 | a0002 | c0002 | t0009 | g0023 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03516 | hp1 | a0001 | c0003 | t0014 | g0102 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0059 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0056 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0080 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0026 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0026 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0049 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0071 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0048 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04228 | hp1 | a0002 | c0002 | t0008 | g0012 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG04228 | hp2 | a0002 | c0002 | t0008 | g0053 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18747 | hp2 | a0001 | c0001 | t0019 | g0172 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0197 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18947 | hp2 | a0001 | c0001 | t0018 | g0156 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18956 | hp2 | a0001 | c0001 | t0024 | g0017 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18970 | hp1 | a0002 | c0007 | t0011 | g0065 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0025 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0132 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19063 | hp1 | a0006 | c0011 | t0001 | g0092 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0038 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0022 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0001 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG03471 | hp2 | a0002 | c0002 | t0011 | g0124 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0082 | REF | REF | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0199 | REF | REF | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113113773 | A | C | 1 | a0006 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.247A>C | p.Ser83Arg | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 3/8 | 298/3063 | 247/1335 | 83/444 | chr13 | 113113773 | |||
| chr13:113115761 | T | G | 1 | a0006 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.466T>G | p.Tyr156Asp | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 517/3063 | 466/1335 | 156/444 | chr13 | 113115761 | |||
| chr13:113118436 | G | C | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.763G>C | p.Asp255His | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 814/3063 | 763/1335 | 255/444 | chr13 | 113118436 | |||
| chr13:113118458 | G | A | 1 | a0005 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.785G>A | p.Arg262Gln | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 836/3063 | 785/1335 | 262/444 | chr13 | 113118458 | |||
| chr13:113118845 | G | A | 1 | a0002 | 37 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(34): Show |
missense_variant | MODERATE | c.1172G>A | p.Arg391Gln | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1223/3063 | 1172/1335 | 391/444 | chr13 | 113118845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113110844 | G | A | 1 | a0001c0004 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.219G>A | p.Glu73Glu | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/8 | 270/3063 | 219/1335 | 73/444 | chr13 | 113110844 | |||
| chr13:113115754 | C | T | 3 | a0001c0003 a0002c0002 a0002c0010 |
42 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
synonymous_variant | LOW | c.459C>T | p.His153His | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 510/3063 | 459/1335 | 153/444 | chr13 | 113115754 | |||
| chr13:113115778 | C | T | 2 | a0001c0009 a0002c0010 |
2 | HG00609.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.483C>T | p.Asp161Asp | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 534/3063 | 483/1335 | 161/444 | chr13 | 113115778 | |||
| chr13:113118975 | C | T | 1 | a0003c0008 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.1302C>T | p.Arg434Arg | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1353/3063 | 1302/1335 | 434/444 | chr13 | 113118975 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113119090 | T | C | 1 | a0002c0002t0008 | 2 | HG04228.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 82 | chr13 | 113119090 | ||||||
| chr13:113119162 | C | CAA | 12 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0012 others(9): Show |
54 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*155_*156insAA | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 156 | INFO_REALIGN_3_PRIME | chr13 | 113119162 | |||||
| chr13:113119166 | G | A | 1 | a0001c0001t0007 | 3 | HG01884.hp2 HG02280.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 158 | chr13 | 113119166 | ||||||
| chr13:113119176 | G | A | 1 | a0001c0001t0018 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 168 | chr13 | 113119176 | ||||||
| chr13:113119365 | C | T | 1 | a0001c0001t0025 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 357 | chr13 | 113119365 | ||||||
| chr13:113119541 | A | C | 1 | a0001c0001t0005 | 5 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 533 | chr13 | 113119541 | ||||||
| chr13:113119606 | GATGCACG others(9): Show |
G | 1 | a0001c0001t0019 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610_*625delTGCCAA others(10): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 610 | INFO_REALIGN_3_PRIME | chr13 | 113119606 | |||||
| chr13:113119628 | C | T | 1 | a0001c0001t0012 | 2 | HG02559.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 620 | chr13 | 113119628 | ||||||
| chr13:113119646 | C | T | 1 | a0001c0001t0024 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 638 | chr13 | 113119646 | ||||||
| chr13:113119647 | G | A | 1 | a0001c0001t0004 | 8 | HG02145.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*639G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 639 | chr13 | 113119647 | ||||||
| chr13:113119681 | A | G | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0017 |
14 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*673A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 673 | chr13 | 113119681 | ||||||
| chr13:113119743 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0020 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756_*767delGATGCA others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 756 | INFO_REALIGN_3_PRIME | chr13 | 113119743 | |||||
| chr13:113119778 | G | A | 5 | a0002c0002t0003 a0002c0002t0008 a0002c0002t0009 others(2): Show |
34 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*770G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 770 | chr13 | 113119778 | ||||||
| chr13:113119896 | G | A | 3 | a0001c0001t0002 a0001c0001t0024 a0003c0008t0002 |
30 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 888 | chr13 | 113119896 | ||||||
| chr13:113119951 | G | A | 1 | a0001c0001t0013 | 2 | HG01243.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*943G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 943 | chr13 | 113119951 | ||||||
| chr13:113120132 | T | C | 1 | a0001c0003t0010 | 2 | HG02630.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1124T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1124 | chr13 | 113120132 | ||||||
| chr13:113120154 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0017 others(1): Show |
16 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1146A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1146 | chr13 | 113120154 | ||||||
| chr13:113120248 | C | G | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1240 | chr13 | 113120248 | ||||||
| chr13:113120283 | A | G | 2 | a0001c0001t0004 a0001c0003t0014 |
10 | HG02145.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1275A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1275 | chr13 | 113120283 | ||||||
| chr13:113120450 | G | A | 1 | a0001c0001t0022 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1442 | chr13 | 113120450 | ||||||
| chr13:113120484 | G | A | 1 | a0002c0010t0015 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1476G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1476 | chr13 | 113120484 | ||||||
| chr13:113120504 | GCACT | G | 2 | a0001c0001t0023 a0002c0002t0009 |
3 | HG02698.hp2 HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500_*1503delTCAC | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1500 | INFO_REALIGN_3_PRIME | chr13 | 113120504 | |||||
| chr13:113120534 | GCACT | G | 1 | a0001c0001t0006 | 4 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1530_*1533delTCAC | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1530 | INFO_REALIGN_3_PRIME | chr13 | 113120534 | |||||
| chr13:113120657 | G | A | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1649 | chr13 | 113120657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113105909 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02809.hp2 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.64+4C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113105909 | |||||||
| chr13:113105914 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0070 others(35): Show |
53 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+9G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113105914 | |||||||
| chr13:113106022 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.64+117G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106022 | |||||||
| chr13:113106101 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.64+196G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106101 | |||||||
| chr13:113106189 | G | A | 1 | a0001c0001t0004g0021 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+284G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106189 | |||||||
| chr13:113106210 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0074 a0001c0001t0001g0075 |
4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+305G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106210 | |||||||
| chr13:113106273 | C | T | 1 | a0001c0001t0018g0156 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64+368C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106273 | |||||||
| chr13:113106305 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0076 |
3 | HG02451.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.64+400G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106305 | |||||||
| chr13:113106335 | G | A | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+430G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106335 | |||||||
| chr13:113106388 | G | A | 1 | a0001c0003t0014g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64+483G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106388 | |||||||
| chr13:113106396 | C | T | 1 | a0002c0002t0003g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+491C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106396 | |||||||
| chr13:113106398 | TG | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0154 others(1): Show |
7 | NA18612.hp1 NA18939.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+500delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106398 | ||||||
| chr13:113106516 | G | C | 1 | a0001c0001t0002g0078 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+611G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106516 | |||||||
| chr13:113106541 | T | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(53): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64+636T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106541 | |||||||
| chr13:113106548 | G | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.64+643G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106548 | |||||||
| chr13:113106553 | C | G | 53 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.64+648C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106553 | |||||||
| chr13:113106565 | A | ATGGAAAG others(4): Show |
1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+662_64+663insGA others(9): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106565 | ||||||
| chr13:113106565 | A | G | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+660A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106565 | |||||||
| chr13:113106583 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+678G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106583 | |||||||
| chr13:113106587 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+682C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106587 | |||||||
| chr13:113106588 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+683A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106588 | |||||||
| chr13:113106589 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+684T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106589 | |||||||
| chr13:113106592 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+687A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106592 | |||||||
| chr13:113106593 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+688A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106593 | |||||||
| chr13:113106595 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+690G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106595 | |||||||
| chr13:113106598 | C | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+693C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106598 | |||||||
| chr13:113106602 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+697T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106602 | |||||||
| chr13:113106607 | T | TGTGGGGA others(49): Show |
1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+703_64+704insTG others(54): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106607 | ||||||
| chr13:113106612 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+707A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106612 | |||||||
| chr13:113106622 | A | ATGGAGGT others(129): Show |
5 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0090 others(2): Show |
5 | HG01433.hp2 HG03098.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106622 | ||||||
| chr13:113106623 | T | G | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+718T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106623 | |||||||
| chr13:113106624 | G | GGAGGTGT others(130): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+720_64+721insAG others(135): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(127): Show |
1 | a0001c0001t0001g0157 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(132): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(128): Show |
34 | a0001c0001t0001g0050 a0001c0001t0004g0022 a0001c0001t0012g0061 others(31): Show |
38 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(127): Show |
1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(132): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(128): Show |
57 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
119 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(129): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18955.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(129): Show |
1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGAGGTGT others(128): Show |
109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | GGGGATGG others(5): Show |
1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+722_64+723insAT others(10): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | ||||||
| chr13:113106624 | G | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+719G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106624 | |||||||
| chr13:113106625 | G | GAGGTGTG others(129): Show |
1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106625 | |||||||
| chr13:113106640 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.64+735C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106640 | |||||||
| chr13:113106723 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+818G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106723 | |||||||
| chr13:113106750 | T | TG | 8 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+851dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106750 | ||||||
| chr13:113106842 | C | T | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+937C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106842 | |||||||
| chr13:113106846 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64+941C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106846 | |||||||
| chr13:113106888 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG01109.hp1 HG02717.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+983G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106888 | |||||||
| chr13:113107199 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
116 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.64+1294C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107199 | |||||||
| chr13:113107245 | GGGTGTCC others(128): Show |
G | 1 | a0001c0001t0023g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+1343_64+1477del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107245 | ||||||
| chr13:113107249 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1344G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107249 | |||||||
| chr13:113107250 | T | G | 1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1345T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107250 | |||||||
| chr13:113107251 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1346C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107251 | |||||||
| chr13:113107254 | GGGAGTGT others(27): Show |
G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0201 others(5): Show |
19 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+1383_64+1416del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107254 | ||||||
| chr13:113107257 | A | AGTGTGGG others(10): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1365_64+1366ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107257 | ||||||
| chr13:113107271 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.64+1366G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107271 | |||||||
| chr13:113107271 | GGGGGCGT others(10): Show |
G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1369_64+1385del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107271 | ||||||
| chr13:113107276 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(43): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1371C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107276 | |||||||
| chr13:113107278 | TGGGTGTC others(163): Show |
T | 1 | a0001c0001t0001g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.64+1383_64+1552del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107278 | ||||||
| chr13:113107287 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1382C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107287 | |||||||
| chr13:113107288 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.64+1383A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107288 | |||||||
| chr13:113107291 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0016g0200 |
2 | HG03209.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.64+1386A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107291 | |||||||
| chr13:113107293 | T | C | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1388T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107293 | |||||||
| chr13:113107304 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.64+1399C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107304 | |||||||
| chr13:113107308 | G | A | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1403G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107308 | |||||||
| chr13:113107309 | G | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1404G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107309 | |||||||
| chr13:113107310 | C | A | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0002c0010t0015g0084 |
5 | HG01496.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1405C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107310 | |||||||
| chr13:113107310 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0016g0200 |
3 | HG03098.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1405C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107310 | |||||||
| chr13:113107310 | CGTGGGTG others(146): Show |
C | 2 | a0001c0001t0004g0178 a0001c0001t0017g0177 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1420_64+1572del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107310 | ||||||
| chr13:113107312 | TGGGTGTC others(129): Show |
T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(35): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+1470_64+1605del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107312 | ||||||
| chr13:113107325 | A | G | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1420A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107325 | |||||||
| chr13:113107327 | T | C | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1422T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107327 | |||||||
| chr13:113107336 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1431C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107336 | |||||||
| chr13:113107339 | G | A | 1 | a0001c0001t0004g0022 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.64+1434G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107339 | |||||||
| chr13:113107341 | G | A | 2 | a0001c0001t0004g0021 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+1436G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107341 | |||||||
| chr13:113107344 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.64+1439C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107344 | |||||||
| chr13:113107345 | G | A | 30 | a0001c0001t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(27): Show |
33 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+1440G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107345 | |||||||
| chr13:113107346 | T | A | 2 | a0001c0001t0004g0021 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+1441T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107346 | |||||||
| chr13:113107346 | TGGGTGTC others(27): Show |
T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0158 others(3): Show |
7 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+1470_64+1503del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107346 | ||||||
| chr13:113107356 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1451G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107356 | |||||||
| chr13:113107369 | TCCCGGAG others(23): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+1465_64+1494del others(30): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107369 | |||||||
| chr13:113107370 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1465C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107370 | |||||||
| chr13:113107373 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(61): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.64+1468G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107373 | |||||||
| chr13:113107375 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.64+1470A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107375 | |||||||
| chr13:113107379 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.64+1474G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107379 | |||||||
| chr13:113107380 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.64+1475A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107380 | |||||||
| chr13:113107390 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1485G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107390 | |||||||
| chr13:113107404 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1499C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107404 | |||||||
| chr13:113107407 | G | A | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1502G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107407 | |||||||
| chr13:113107409 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
6 | HG01496.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1504G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107409 | |||||||
| chr13:113107412 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.64+1507A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107412 | |||||||
| chr13:113107412 | A | T | 1 | a0001c0001t0023g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+1507A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107412 | |||||||
| chr13:113107414 | T | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
6 | HG01496.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1509T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107414 | |||||||
| chr13:113107414 | T | TGGGTGTC others(10): Show |
1 | a0001c0001t0001g0030 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.64+1525_64+1526ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107414 | ||||||
| chr13:113107438 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1533C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107438 | |||||||
| chr13:113107441 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1536G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107441 | |||||||
| chr13:113107443 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0070 others(15): Show |
32 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+1538A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107443 | |||||||
| chr13:113107446 | C | A | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1541C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107446 | |||||||
| chr13:113107448 | A | AG | 6 | a0001c0001t0001g0088 a0001c0001t0002g0078 a0001c0001t0002g0083 others(3): Show |
6 | HG01928.hp2 HG04115.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+1546dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | ||||||
| chr13:113107448 | A | AGGGTGTC others(96): Show |
1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | ||||||
| chr13:113107448 | A | AGGGTGTC others(200): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(207): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | ||||||
| chr13:113107448 | A | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0070 others(13): Show |
30 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+1543A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107448 | |||||||
| chr13:113107453 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1548G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107453 | |||||||
| chr13:113107458 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1553G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107458 | |||||||
| chr13:113107460 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1555G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107460 | |||||||
| chr13:113107461 | A | G | 1 | a0001c0001t0002g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.64+1556A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107461 | |||||||
| chr13:113107467 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1562G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107467 | |||||||
| chr13:113107475 | G | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0158 others(7): Show |
11 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+1570G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107475 | |||||||
| chr13:113107479 | G | GAGTGGGT others(78): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1574_64+1575ins others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107479 | |||||||
| chr13:113107479 | G | GCGTGGGT others(62): Show |
1 | a0001c0001t0001g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(69): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107479 | ||||||
| chr13:113107479 | G | T | 1 | a0001c0001t0002g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.64+1574G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107479 | |||||||
| chr13:113107480 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1575C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107480 | |||||||
| chr13:113107482 | T | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1577T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107482 | |||||||
| chr13:113107495 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
7 | HG01516.hp1 HG02602.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+1590A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107495 | |||||||
| chr13:113107497 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1592T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107497 | |||||||
| chr13:113107497 | TGTGGGTG others(485): Show |
T | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1593_64+2084del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107497 | |||||||
| chr13:113107499 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1594T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107499 | |||||||
| chr13:113107506 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1601C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107506 | |||||||
| chr13:113107508 | C | CA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1603_64+1604ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107508 | |||||||
| chr13:113107511 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1606G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107511 | |||||||
| chr13:113107513 | G | GCGAGGGG others(29): Show |
1 | a0001c0001t0001g0099 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(29): Show |
1 | a0001c0001t0002g0089 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(29): Show |
1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(28): Show |
3 | a0001c0001t0001g0107 a0001c0001t0004g0108 a0006c0011t0001g0092 |
3 | HG00544.hp2 HG03195.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.64+1608_64+1609ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(27): Show |
1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(28): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GCGAGGGT others(29): Show |
1 | a0002c0002t0003g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | GTGTGGGT others(11): Show |
1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107513 | G | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1608G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | |||||||
| chr13:113107514 | A | AGGGTGTC others(26): Show |
1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.64+1610_64+1611ins others(33): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107514 | ||||||
| chr13:113107514 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.64+1609A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107514 | |||||||
| chr13:113107516 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.64+1611T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107516 | |||||||
| chr13:113107522 | T | TCCCGGGG others(28): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1623_64+1624ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107522 | ||||||
| chr13:113107525 | C | G | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1620C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107525 | |||||||
| chr13:113107529 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.64+1624A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107529 | |||||||
| chr13:113107540 | C | CCCGGGGG others(27): Show |
1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1639_64+1640ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107540 | ||||||
| chr13:113107540 | C | T | 2 | a0001c0003t0010g0042 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1635C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107540 | |||||||
| chr13:113107542 | C | CA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.64+1637_64+1638ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107542 | |||||||
| chr13:113107543 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0158 others(6): Show |
10 | HG01496.hp2 HG02129.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+1638G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107543 | |||||||
| chr13:113107545 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.64+1640A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107545 | |||||||
| chr13:113107547 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.64+1642G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107547 | |||||||
| chr13:113107550 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+1645A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107550 | |||||||
| chr13:113107550 | A | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.64+1645A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107550 | |||||||
| chr13:113107565 | T | C | 1 | a0001c0003t0014g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.64+1660T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107565 | |||||||
| chr13:113107577 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(35): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+1672G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107577 | |||||||
| chr13:113107582 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.64+1677A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107582 | |||||||
| chr13:113107589 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1684G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107589 | |||||||
| chr13:113107590 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1685T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107590 | |||||||
| chr13:113107591 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1686C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107591 | |||||||
| chr13:113107593 | C | G | 8 | a0001c0001t0001g0106 a0001c0001t0002g0150 a0001c0001t0004g0022 others(5): Show |
9 | HG00673.hp1 HG02735.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1688C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107593 | |||||||
| chr13:113107608 | C | CCCGGGGG others(27): Show |
1 | a0001c0001t0001g0050 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64+1707_64+1708ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107608 | ||||||
| chr13:113107608 | C | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0106 others(13): Show |
28 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.64+1703C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107608 | |||||||
| chr13:113107613 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.64+1708A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107613 | |||||||
| chr13:113107618 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64+1713A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107618 | |||||||
| chr13:113107618 | A | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.64+1713A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107618 | |||||||
| chr13:113107627 | C | G | 43 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0095 others(40): Show |
47 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+1722C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107627 | |||||||
| chr13:113107631 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1726A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107631 | |||||||
| chr13:113107633 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.64+1728T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107633 | |||||||
| chr13:113107633 | TGTGGGTG others(27): Show |
T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1762_64+1795del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107633 | ||||||
| chr13:113107642 | C | T | 43 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0095 others(40): Show |
47 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+1737C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107642 | |||||||
| chr13:113107645 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(38): Show |
90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.64+1740G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107645 | |||||||
| chr13:113107647 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
138 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.64+1742G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107647 | |||||||
| chr13:113107647 | GGGCGTGG others(113): Show |
G | 1 | a0001c0001t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+1744_64+1863del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107647 | ||||||
| chr13:113107649 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1744G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107649 | |||||||
| chr13:113107650 | C | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0070 others(13): Show |
28 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.64+1745C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107650 | |||||||
| chr13:113107650 | CGTGGGTG others(112): Show |
C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG03098.hp2 HG03471.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.64+1762_64+1880del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107650 | ||||||
| chr13:113107652 | T | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(81): Show |
137 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.64+1747T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107652 | |||||||
| chr13:113107652 | T | G | 1 | a0002c0002t0003g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64+1747T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107652 | |||||||
| chr13:113107654 | G | GGTGTCCG others(27): Show |
1 | a0001c0001t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64+1755_64+1756ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107654 | ||||||
| chr13:113107655 | G | GTGTCCGG others(28): Show |
1 | a0001c0001t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.64+1755_64+1756ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107655 | ||||||
| chr13:113107661 | C | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1756C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107661 | |||||||
| chr13:113107667 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.64+1762C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107667 | |||||||
| chr13:113107676 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.64+1771C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107676 | |||||||
| chr13:113107681 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.64+1776G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107681 | |||||||
| chr13:113107684 | C | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0088 others(46): Show |
54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1779C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107684 | |||||||
| chr13:113107686 | T | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.64+1781T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107686 | |||||||
| chr13:113107686 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+1781T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107686 | |||||||
| chr13:113107695 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64+1790C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107695 | |||||||
| chr13:113107710 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1805C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107710 | |||||||
| chr13:113107713 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.64+1808G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107713 | |||||||
| chr13:113107715 | G | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0088 others(46): Show |
54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1810G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107715 | |||||||
| chr13:113107716 | GGCGTGGG others(44): Show |
G | 1 | a0001c0001t0001g0007 | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1813_64+1863del others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107716 | ||||||
| chr13:113107718 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1813C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107718 | |||||||
| chr13:113107720 | T | A | 49 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0088 others(46): Show |
54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1815T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107720 | |||||||
| chr13:113107720 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1815T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107720 | |||||||
| chr13:113107720 | TGGGTGTC others(469): Show |
T | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+1839_64+2314del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107720 | ||||||
| chr13:113107735 | TGTGGGTG others(129): Show |
T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0158 a0001c0001t0001g0165 others(1): Show |
5 | HG02129.hp2 HG02132.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1839_64+1974del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107735 | ||||||
| chr13:113107739 | G | C | 3 | a0001c0001t0001g0105 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1834G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107739 | |||||||
| chr13:113107749 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1844G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107749 | |||||||
| chr13:113107750 | GGCGTGGG others(10): Show |
G | 14 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0001g0201 others(11): Show |
18 | HG00673.hp1 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+1847_64+1863del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107750 | ||||||
| chr13:113107752 | C | CGAGGGGT others(45): Show |
1 | a0001c0001t0001g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.64+1848_64+1849ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107752 | ||||||
| chr13:113107752 | C | CGAGGGTG others(46): Show |
1 | a0001c0001t0001g0110 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+1848_64+1849ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107752 | ||||||
| chr13:113107754 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.64+1849T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107754 | |||||||
| chr13:113107754 | T | G | 1 | a0004c0005t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+1849T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107754 | |||||||
| chr13:113107763 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1858C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107763 | |||||||
| chr13:113107763 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1858C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107763 | |||||||
| chr13:113107767 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG00733.hp2 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+1862A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107767 | |||||||
| chr13:113107769 | T | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0070 others(14): Show |
29 | HG00673.hp1 HG00733.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+1864T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107769 | |||||||
| chr13:113107769 | T | C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0159 a0001c0001t0016g0200 others(1): Show |
5 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1864T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107769 | |||||||
| chr13:113107769 | T | TGTGGGGT others(11): Show |
1 | a0001c0003t0001g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.64+1869_64+1870ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(10): Show |
40 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0095 others(37): Show |
44 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(10): Show |
1 | a0001c0001t0001g0101 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(44): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(45): Show |
1 | a0004c0005t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(44): Show |
1 | a0001c0001t0001g0142 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107769 | T | TGTGGGTG others(146): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1872_64+1873ins others(153): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | ||||||
| chr13:113107771 | T | TGGGTGTC others(11): Show |
2 | a0001c0001t0001g0088 a0002c0002t0003g0198 |
2 | NA19054.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107771 | ||||||
| chr13:113107771 | T | TGGGTGTC others(249): Show |
1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(256): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107771 | ||||||
| chr13:113107776 | G | GTCCCGGG others(11): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107776 | ||||||
| chr13:113107778 | C | CCCGGGGG others(9): Show |
1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107778 | ||||||
| chr13:113107778 | CCCGGGAG others(10): Show |
C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(39): Show |
91 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+1878_64+1894del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107778 | ||||||
| chr13:113107780 | C | T | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1875C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107780 | |||||||
| chr13:113107784 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0016g0200 a0001c0003t0010g0042 others(1): Show |
5 | HG00544.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1879A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107784 | |||||||
| chr13:113107786 | T | A | 2 | a0001c0001t0001g0107 a0006c0011t0001g0092 |
2 | HG00544.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.64+1881T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107786 | |||||||
| chr13:113107786 | T | C | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1881T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107786 | |||||||
| chr13:113107795 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0167 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1890T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107795 | |||||||
| chr13:113107805 | A | AG | 4 | a0001c0001t0001g0107 a0001c0001t0001g0145 a0001c0001t0001g0155 others(1): Show |
4 | HG00544.hp2 HG03710.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1903dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107805 | ||||||
| chr13:113107808 | GTGTCCCG others(9): Show |
G | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+1904_64+1919del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107808 | |||||||
| chr13:113107810 | G | A | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1905G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107810 | |||||||
| chr13:113107815 | G | A | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1910G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107815 | |||||||
| chr13:113107817 | G | A | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1912G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107817 | |||||||
| chr13:113107820 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64+1915T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107820 | |||||||
| chr13:113107820 | T | TGTGAGTG others(10): Show |
1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1918_64+1919ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107820 | ||||||
| chr13:113107820 | TGTGCGTG others(10): Show |
T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(41): Show |
93 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.64+1919_64+1935del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107820 | ||||||
| chr13:113107824 | C | A | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1919C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107824 | |||||||
| chr13:113107824 | C | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0151 a0001c0001t0016g0200 |
3 | HG02080.hp2 HG03209.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.64+1919C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107824 | |||||||
| chr13:113107832 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0022g0001 a0001c0003t0010g0042 |
9 | HG01069.hp2 HG01106.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1927G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107832 | |||||||
| chr13:113107835 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+1930G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107835 | |||||||
| chr13:113107837 | C | CGTGGGTG others(10): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1946_64+1947ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107837 | ||||||
| chr13:113107837 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0016g0200 |
2 | HG03209.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.64+1932C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107837 | |||||||
| chr13:113107839 | TGGGTGTC others(350): Show |
T | 1 | a0001c0001t0001g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.64+1947_64+2303del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107839 | ||||||
| chr13:113107854 | C | T | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1949C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107854 | |||||||
| chr13:113107857 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64+1952G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107857 | |||||||
| chr13:113107859 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1954G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107859 | |||||||
| chr13:113107866 | G | A | 1 | a0002c0002t0021g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+1961G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107866 | |||||||
| chr13:113107869 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(44): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1964G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107869 | |||||||
| chr13:113107871 | C | CGTGGGTG others(10): Show |
1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1974_64+1975ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107871 | ||||||
| chr13:113107871 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(44): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1966C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107871 | |||||||
| chr13:113107883 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(46): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.64+1978G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107883 | |||||||
| chr13:113107888 | C | T | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1983C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107888 | |||||||
| chr13:113107890 | A | AGGGTGTC others(727): Show |
1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1989_64+1990ins others(734): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107890 | ||||||
| chr13:113107895 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0016g0200 others(1): Show |
13 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+1990A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107895 | |||||||
| chr13:113107900 | A | G | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1995A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107900 | |||||||
| chr13:113107902 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1997A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107902 | |||||||
| chr13:113107903 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1998A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107903 | |||||||
| chr13:113107909 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2004A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107909 | |||||||
| chr13:113107914 | C | T | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2009C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107914 | |||||||
| chr13:113107917 | A | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.64+2012A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107917 | |||||||
| chr13:113107919 | G | A | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2014G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107919 | |||||||
| chr13:113107922 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(46): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.64+2017C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107922 | |||||||
| chr13:113107924 | T | A | 2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2019T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107924 | |||||||
| chr13:113107933 | C | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2028C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107933 | |||||||
| chr13:113107937 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2032G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107937 | |||||||
| chr13:113107939 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2034T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | |||||||
| chr13:113107939 | TGTGGGTG others(9): Show |
T | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2035_64+2050del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | |||||||
| chr13:113107939 | TGTGGGTG others(43): Show |
T | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2035_64+2084del others(50): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | |||||||
| chr13:113107939 | TGTGGGTG others(247): Show |
T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(38): Show |
90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.64+2035_64+2288del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | |||||||
| chr13:113107939 | TGTGGGTG others(367): Show |
T | 1 | a0001c0001t0001g0047 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.64+2035_65-2377del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | |||||||
| chr13:113107955 | G | GCGTGGGT others(11): Show |
2 | a0001c0001t0016g0200 a0001c0003t0010g0042 |
3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2065_64+2066ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107955 | ||||||
| chr13:113107956 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+2051C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107956 | |||||||
| chr13:113107956 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2051C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107956 | |||||||
| chr13:113107971 | A | G | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2066A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107971 | |||||||
| chr13:113107972 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64+2067G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107972 | |||||||
| chr13:113107973 | TGTGGGTG others(9): Show |
T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2069_64+2084del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107973 | |||||||
| chr13:113107982 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2077T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107982 | |||||||
| chr13:113107985 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64+2080G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107985 | |||||||
| chr13:113107987 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0139 |
2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2082A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107987 | |||||||
| chr13:113107990 | T | C | 18 | a0001c0001t0001g0035 a0001c0001t0001g0104 a0001c0001t0001g0105 others(15): Show |
20 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.64+2085T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107990 | |||||||
| chr13:113107992 | A | T | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 others(5): Show |
8 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+2087A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107992 | |||||||
| chr13:113108001 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.64+2096C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108001 | |||||||
| chr13:113108016 | T | C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01261.hp1 HG01261.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+2111T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108016 | |||||||
| chr13:113108019 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0123 |
5 | HG01358.hp1 HG01361.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2114G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108019 | |||||||
| chr13:113108021 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0139 a0001c0001t0001g0158 |
3 | HG01934.hp1 HG02293.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.64+2116A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108021 | |||||||
| chr13:113108026 | A | AGGGTGTC others(27): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0139 |
2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2133_64+2134ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108026 | ||||||
| chr13:113108026 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2121A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108026 | |||||||
| chr13:113108032 | TCCCGGGA others(11): Show |
T | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2130_64+2147del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108032 | ||||||
| chr13:113108041 | T | TGTGGGGT others(11): Show |
1 | a0001c0001t0001g0002 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.64+2141_64+2142ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108041 | ||||||
| chr13:113108041 | T | TGTGGGTT others(12): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+2142_64+2143ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108041 | ||||||
| chr13:113108050 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0139 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2145C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108050 | |||||||
| chr13:113108052 | C | G | 1 | a0002c0002t0003g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+2147C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108052 | |||||||
| chr13:113108053 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2148G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108053 | |||||||
| chr13:113108055 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2150G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108055 | |||||||
| chr13:113108057 | G | GCGTGGGT others(11): Show |
144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.64+2167_64+2168ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | ||||||
| chr13:113108057 | G | GCGTGGGT others(45): Show |
1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | ||||||
| chr13:113108057 | G | GCGTGGGT others(12): Show |
1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64+2159_64+2160ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | ||||||
| chr13:113108058 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2153C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108058 | |||||||
| chr13:113108058 | CGTGGGTG others(300): Show |
C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0193 |
2 | NA18612.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.64+2168_65-2311del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108058 | ||||||
| chr13:113108060 | T | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0139 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2155T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108060 | |||||||
| chr13:113108061 | G | GGGTGTCC others(10): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108061 | ||||||
| chr13:113108069 | C | CGGGGGTC others(11): Show |
1 | a0001c0001t0002g0002 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108069 | ||||||
| chr13:113108070 | GGGAGTGT others(316): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2168_65-2295del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108070 | ||||||
| chr13:113108071 | GGAGTGTG others(77): Show |
G | 2 | a0001c0001t0001g0040 a0002c0002t0003g0056 |
3 | HG01978.hp1 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+2168_64+2251del others(84): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108071 | ||||||
| chr13:113108073 | A | G | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2168A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108073 | |||||||
| chr13:113108075 | T | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2170T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108075 | |||||||
| chr13:113108077 | TGGGTGTT others(10): Show |
T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2179_64+2195del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108077 | ||||||
| chr13:113108084 | T | C | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2179T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108084 | |||||||
| chr13:113108086 | C | T | 1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2181C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108086 | |||||||
| chr13:113108087 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0139 |
2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2182G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108087 | |||||||
| chr13:113108089 | A | G | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2184A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108089 | |||||||
| chr13:113108090 | G | A | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2185G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108090 | |||||||
| chr13:113108092 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.64+2187T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108092 | |||||||
| chr13:113108092 | T | TC | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(2): Show |
5 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2187_64+2188ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108092 | |||||||
| chr13:113108094 | A | T | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2189A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108094 | |||||||
| chr13:113108101 | C | T | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2196C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108101 | |||||||
| chr13:113108104 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2199G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108104 | |||||||
| chr13:113108106 | G | A | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2201G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108106 | |||||||
| chr13:113108107 | A | G | 2 | a0002c0002t0003g0063 a0002c0010t0015g0084 |
2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.64+2202A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108107 | |||||||
| chr13:113108109 | T | C | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2204T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108109 | |||||||
| chr13:113108111 | T | A | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2206T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108111 | |||||||
| chr13:113108118 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
8 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+2213T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108118 | |||||||
| chr13:113108123 | A | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(4): Show |
7 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2218A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108123 | |||||||
| chr13:113108124 | G | A | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2219G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108124 | |||||||
| chr13:113108126 | C | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2221C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108126 | |||||||
| chr13:113108126 | C | T | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2221C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108126 | |||||||
| chr13:113108128 | A | AG | 5 | a0001c0001t0001g0090 a0001c0001t0001g0116 a0001c0001t0002g0078 others(2): Show |
5 | HG03098.hp1 HG03942.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2226dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108128 | ||||||
| chr13:113108128 | A | AGGGTGTC others(44): Show |
1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2249_64+2250ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108128 | ||||||
| chr13:113108128 | A | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(4): Show |
7 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2223A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108128 | |||||||
| chr13:113108141 | A | AGTGTGGG others(10): Show |
3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2249_64+2250ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108141 | ||||||
| chr13:113108141 | A | G | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2236A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108141 | |||||||
| chr13:113108143 | T | C | 1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2238T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108143 | |||||||
| chr13:113108143 | T | TGTGGGTG others(44): Show |
1 | a0001c0001t0001g0007 | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+2246_64+2247ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108143 | ||||||
| chr13:113108152 | CCCAGGGG others(350): Show |
C | 1 | a0001c0001t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+2250_65-2179del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108152 | ||||||
| chr13:113108155 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64+2250A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108155 | |||||||
| chr13:113108155 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.64+2250A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108155 | |||||||
| chr13:113108158 | GGCGTGGG others(351): Show |
G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+2270_65-2158del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108158 | ||||||
| chr13:113108159 | G | GCGTGGGT others(11): Show |
147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.64+2269_64+2270ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108159 | ||||||
| chr13:113108159 | G | GCGTGGGT others(13): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+2261_64+2262ins others(20): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108159 | ||||||
| chr13:113108159 | G | GGCGTGGG others(12): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0136 |
2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.64+2254_64+2255ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | |||||||
| chr13:113108159 | G | GT | 2 | a0001c0001t0001g0007 a0002c0002t0003g0063 |
10 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+2254_64+2255ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | |||||||
| chr13:113108159 | G | T | 2 | a0001c0001t0001g0040 a0002c0002t0003g0056 |
3 | HG01978.hp1 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+2254G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | |||||||
| chr13:113108160 | C | A | 1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2255C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108160 | |||||||
| chr13:113108160 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2255C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108160 | |||||||
| chr13:113108162 | T | TGGGTGTT others(10): Show |
1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2263_64+2264ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108162 | ||||||
| chr13:113108168 | T | TCCCGGGG others(12): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+2269_64+2270ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108168 | ||||||
| chr13:113108171 | C | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0171 |
2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+2266C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108171 | |||||||
| chr13:113108172 | GGGAGTGT others(350): Show |
G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0171 |
2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+2270_65-2159del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108172 | ||||||
| chr13:113108175 | A | G | 1 | a0001c0001t0004g0021 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+2270A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108175 | |||||||
| chr13:113108177 | TGTGGGTG others(9): Show |
T | 1 | a0001c0001t0004g0021 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+2273_64+2288del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108177 | |||||||
| chr13:113108186 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2281T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108186 | |||||||
| chr13:113108188 | C | T | 32 | a0001c0001t0001g0050 a0001c0001t0012g0061 a0001c0001t0012g0062 others(29): Show |
35 | HG00673.hp1 HG01496.hp2 HG01515.hp2 others(32): Show |
intron_variant | MODIFIER | c.64+2283C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108188 | |||||||
| chr13:113108191 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2286A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108191 | |||||||
| chr13:113108194 | C | A | 3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2289C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108194 | |||||||
| chr13:113108196 | A | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(42): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+2291A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108196 | |||||||
| chr13:113108206 | G | A | 1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2301G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108206 | |||||||
| chr13:113108220 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(39): Show |
91 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+2315T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108220 | |||||||
| chr13:113108223 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0165 others(1): Show |
5 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2318G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108223 | |||||||
| chr13:113108225 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0165 |
4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2320A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108225 | |||||||
| chr13:113108228 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2323C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108228 | |||||||
| chr13:113108230 | A | AG | 4 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG03927.hp1 HG03927.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2328dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108230 | ||||||
| chr13:113108230 | A | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0165 |
4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2325A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108230 | |||||||
| chr13:113108235 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2330G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108235 | |||||||
| chr13:113108239 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0165 |
3 | HG02129.hp2 HG02132.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.64+2334C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108239 | |||||||
| chr13:113108240 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0194 others(3): Show |
7 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2335G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108240 | |||||||
| chr13:113108242 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2337G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108242 | |||||||
| chr13:113108243 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0165 |
4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2338A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108243 | |||||||
| chr13:113108244 | G | A | 1 | a0002c0002t0009g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.64+2339G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108244 | |||||||
| chr13:113108245 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0165 others(1): Show |
5 | HG02129.hp2 HG02132.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2340T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108245 | |||||||
| chr13:113108247 | T | TGGGTGTT others(10): Show |
3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2348_64+2349ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108247 | ||||||
| chr13:113108249 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2344G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108249 | |||||||
| chr13:113108257 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0016g0200 a0001c0003t0010g0042 |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2352G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108257 | |||||||
| chr13:113108260 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0142 a0001c0001t0016g0200 others(1): Show |
5 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2355G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108260 | |||||||
| chr13:113108260 | G | GGTGTGGG others(129): Show |
1 | a0001c0001t0001g0140 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+2356_64+2357ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108260 | ||||||
| chr13:113108261 | GCGTGGGT others(95): Show |
G | 1 | a0001c0001t0001g0189 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.64+2357_65-2327del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108261 | |||||||
| chr13:113108262 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.64+2357C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108262 | |||||||
| chr13:113108262 | CGTGGGTG others(96): Show |
C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(35): Show |
86 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.64+2375_65-2308del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108262 | ||||||
| chr13:113108274 | G | GGGAGTGT others(111): Show |
1 | a0001c0001t0001g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.64+2371_64+2372ins others(118): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108274 | ||||||
| chr13:113108277 | G | A | 1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2372G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108277 | |||||||
| chr13:113108278 | GT | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.64+2375delT | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108278 | ||||||
| chr13:113108279 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | HG00544.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.64+2374T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108279 | T | TGTGGGGT others(130): Show |
1 | a0001c0001t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108279 | T | TGTGGGTG others(26): Show |
14 | a0001c0001t0001g0015 a0001c0003t0001g0051 a0001c0003t0001g0054 others(11): Show |
17 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.64+2374_64+2375ins others(33): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108279 | T | TGTGGGTG others(130): Show |
1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108279 | T | TGTGGGTG others(129): Show |
1 | a0002c0002t0003g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108279 | T | TGTGGGTG others(129): Show |
1 | a0001c0001t0002g0078 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | |||||||
| chr13:113108280 | T | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0003t0001g0051 others(12): Show |
18 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+2375T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | |||||||
| chr13:113108280 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0043 others(23): Show |
40 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.64+2375T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | |||||||
| chr13:113108280 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2375T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | |||||||
| chr13:113108281 | G | T | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2376G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108281 | |||||||
| chr13:113108282 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2377T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108282 | |||||||
| chr13:113108295 | A | G | 2 | a0001c0001t0001g0032 a0002c0002t0003g0052 |
3 | HG03239.hp2 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.64+2390A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108295 | |||||||
| chr13:113108297 | T | A | 1 | a0002c0002t0003g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2392T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108297 | |||||||
| chr13:113108297 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2392T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108297 | |||||||
| chr13:113108299 | T | TGGGTGTT others(10): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2377_65-2376ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108299 | ||||||
| chr13:113108306 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.65-2384T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108306 | |||||||
| chr13:113108308 | C | T | 1 | a0002c0002t0003g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-2382C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108308 | |||||||
| chr13:113108311 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.65-2379A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108311 | |||||||
| chr13:113108314 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.65-2376C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108314 | |||||||
| chr13:113108316 | A | AGGGTGTC others(95): Show |
1 | a0001c0001t0001g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-2365_65-2364ins others(102): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108316 | ||||||
| chr13:113108316 | A | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.65-2374A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108316 | |||||||
| chr13:113108326 | G | A | 14 | a0001c0001t0001g0015 a0001c0003t0001g0051 a0001c0003t0001g0054 others(11): Show |
17 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-2364G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108326 | |||||||
| chr13:113108331 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0006g0029 others(4): Show |
12 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2359T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108331 | |||||||
| chr13:113108333 | TGGGTGTT others(10): Show |
T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0165 |
4 | HG02129.hp2 HG02132.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2350_65-2334del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108333 | ||||||
| chr13:113108340 | T | C | 13 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0117 others(10): Show |
15 | HG00544.hp1 HG01934.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-2350T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108340 | |||||||
| chr13:113108340 | T | TCCGGAGG others(128): Show |
1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(135): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108340 | ||||||
| chr13:113108340 | T | TCCGGAGG others(130): Show |
1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108340 | ||||||
| chr13:113108345 | A | C | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2345A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108345 | |||||||
| chr13:113108345 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2345A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108345 | |||||||
| chr13:113108350 | A | AGGGTGTC others(95): Show |
1 | a0001c0001t0018g0156 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(102): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | ||||||
| chr13:113108350 | A | AGGGTGTC others(131): Show |
1 | a0001c0001t0001g0113 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | ||||||
| chr13:113108350 | A | AGGGTGTC others(96): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | ||||||
| chr13:113108350 | A | AGGGTGTC others(59): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2329_65-2328ins others(66): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | ||||||
| chr13:113108350 | A | T | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2340A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108350 | |||||||
| chr13:113108352 | G | A | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.65-2338G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108352 | |||||||
| chr13:113108353 | G | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-2337G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108353 | |||||||
| chr13:113108356 | T | TCCCAGGA others(130): Show |
1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108356 | ||||||
| chr13:113108360 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.65-2330G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108360 | |||||||
| chr13:113108363 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0165 others(1): Show |
5 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2327A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108363 | |||||||
| chr13:113108365 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.65-2325T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108365 | |||||||
| chr13:113108367 | T | TGGGTGTT others(10): Show |
1 | a0001c0001t0004g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-2317_65-2316ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108367 | ||||||
| chr13:113108367 | T | TGGGTGTT others(10): Show |
1 | a0001c0001t0001g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-2317_65-2316ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108367 | ||||||
| chr13:113108374 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.65-2316C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108374 | |||||||
| chr13:113108377 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0004g0135 a0002c0010t0015g0084 |
3 | HG01496.hp2 HG02451.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-2313G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108377 | |||||||
| chr13:113108378 | G | GAGGCGA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.65-2312_65-2311ins others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108378 | |||||||
| chr13:113108379 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0018g0156 |
2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2311G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108379 | |||||||
| chr13:113108380 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0004g0135 |
2 | HG02451.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-2310G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108380 | |||||||
| chr13:113108382 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2308T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108382 | |||||||
| chr13:113108382 | T | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.65-2308T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108382 | |||||||
| chr13:113108382 | T | TGTCCCAG others(4): Show |
114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.65-2306_65-2305ins others(11): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108382 | ||||||
| chr13:113108384 | T | A | 2 | a0001c0001t0002g0083 a0001c0001t0018g0156 |
2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2306T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108384 | |||||||
| chr13:113108384 | T | TCCCAGGA others(5): Show |
1 | a0001c0001t0001g0030 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.65-2306_65-2305ins others(12): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108384 | |||||||
| chr13:113108397 | G | A | 17 | a0001c0001t0001g0086 a0001c0001t0002g0083 a0001c0001t0004g0194 others(14): Show |
18 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-2293G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108397 | |||||||
| chr13:113108398 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.65-2292G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108398 | |||||||
| chr13:113108399 | T | A | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2291T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | |||||||
| chr13:113108399 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.65-2291T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | |||||||
| chr13:113108399 | T | TC | 59 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(56): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-2291_65-2290ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | |||||||
| chr13:113108408 | C | CCCGGAGG others(27): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2278_65-2277ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108408 | ||||||
| chr13:113108410 | C | T | 1 | a0002c0002t0003g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-2280C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108410 | |||||||
| chr13:113108411 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2279G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108411 | |||||||
| chr13:113108414 | A | G | 18 | a0001c0001t0001g0047 a0001c0001t0001g0086 a0001c0001t0002g0083 others(15): Show |
20 | HG01496.hp2 HG01515.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.65-2276A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108414 | |||||||
| chr13:113108416 | T | A | 13 | a0001c0003t0001g0051 a0001c0003t0001g0054 a0002c0002t0003g0012 others(10): Show |
14 | HG01515.hp2 HG01517.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-2274T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108416 | |||||||
| chr13:113108416 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0002g0083 a0001c0001t0018g0156 |
3 | NA18947.hp2 NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2274T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108416 | |||||||
| chr13:113108425 | C | T | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2265C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108425 | |||||||
| chr13:113108427 | C | CGGAGGCG others(45): Show |
1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2261_65-2260ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108427 | ||||||
| chr13:113108428 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2262G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108428 | |||||||
| chr13:113108430 | G | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2260G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108430 | |||||||
| chr13:113108431 | GGAGTGGG others(78): Show |
G | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2257_65-2173del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108431 | ||||||
| chr13:113108432 | G | GT | 3 | a0001c0001t0001g0086 a0001c0001t0002g0083 a0001c0001t0018g0156 |
3 | NA18947.hp2 NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2258_65-2257ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108432 | |||||||
| chr13:113108432 | G | T | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2258G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108432 | |||||||
| chr13:113108433 | A | AGTGGGTG others(96): Show |
1 | a0002c0002t0003g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.65-2243_65-2242ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108433 | ||||||
| chr13:113108433 | A | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
22 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-2257A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108433 | |||||||
| chr13:113108435 | T | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2255T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108435 | |||||||
| chr13:113108452 | TGGGTGTT others(44): Show |
T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(43): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.65-2231_65-2181del others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108452 | ||||||
| chr13:113108459 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.65-2231T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108459 | |||||||
| chr13:113108462 | G | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2228G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108462 | |||||||
| chr13:113108479 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.65-2211A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108479 | |||||||
| chr13:113108484 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.65-2206C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108484 | |||||||
| chr13:113108493 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0040 others(15): Show |
32 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-2197C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108493 | |||||||
| chr13:113108496 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0002g0083 others(2): Show |
7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2194G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108496 | |||||||
| chr13:113108498 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.65-2192A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108498 | |||||||
| chr13:113108501 | C | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2189C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108501 | |||||||
| chr13:113108501 | C | CGTGGGTG others(96): Show |
1 | a0001c0001t0001g0032 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.65-2188_65-2187ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108501 | ||||||
| chr13:113108503 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.65-2187A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108503 | |||||||
| chr13:113108513 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.65-2177G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108513 | |||||||
| chr13:113108513 | G | GGGGGTCG others(131): Show |
1 | a0002c0002t0003g0049 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | ||||||
| chr13:113108513 | G | GGGGGTCG others(131): Show |
1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | ||||||
| chr13:113108513 | G | GGGGGTCG others(130): Show |
120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.65-2175_65-2174ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | ||||||
| chr13:113108513 | G | GGGGGTCG others(131): Show |
1 | a0002c0002t0003g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | ||||||
| chr13:113108513 | G | GGGGGTCG others(148): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG01109.hp1 HG02717.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2175_65-2174ins others(155): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | ||||||
| chr13:113108516 | A | AGTGTGGG others(10): Show |
15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(12): Show |
16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2173_65-2172ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108516 | ||||||
| chr13:113108516 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.65-2174A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108516 | |||||||
| chr13:113108518 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0002g0083 others(3): Show |
8 | HG01496.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-2172C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108518 | |||||||
| chr13:113108519 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0151 |
3 | NA18945.hp2 NA19070.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.65-2171G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108519 | |||||||
| chr13:113108529 | C | CGGGAGTG others(130): Show |
2 | a0001c0001t0001g0118 a0004c0005t0001g0141 |
2 | HG02809.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.65-2158_65-2157ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108529 | ||||||
| chr13:113108529 | C | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.65-2161C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108529 | |||||||
| chr13:113108535 | C | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0002g0083 others(2): Show |
7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2155C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108535 | |||||||
| chr13:113108550 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.65-2140A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108550 | |||||||
| chr13:113108563 | C | CAGGGGCG others(45): Show |
2 | a0001c0001t0001g0015 a0002c0002t0003g0063 |
4 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2127_65-2126ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | |||||||
| chr13:113108563 | C | CAGGGGCG others(46): Show |
1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | |||||||
| chr13:113108563 | C | CAGGGGCG others(46): Show |
1 | a0001c0001t0018g0156 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | |||||||
| chr13:113108563 | C | CAGGGGCG others(47): Show |
1 | a0001c0001t0002g0083 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(54): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | |||||||
| chr13:113108568 | G | GT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.65-2122_65-2121ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108568 | |||||||
| chr13:113108568 | G | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0002g0083 others(2): Show |
7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2122G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108568 | |||||||
| chr13:113108569 | A | AGTGGGTG others(267): Show |
3 | a0001c0001t0004g0021 a0001c0001t0005g0013 a0001c0001t0005g0069 |
6 | HG02280.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108569 | ||||||
| chr13:113108569 | A | AGTGGGTG others(267): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0139 |
3 | HG01934.hp1 HG02080.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108569 | ||||||
| chr13:113108569 | A | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.65-2121A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108569 | |||||||
| chr13:113108569 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0110 |
4 | HG02698.hp1 NA18951.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2121A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108569 | |||||||
| chr13:113108584 | A | AGTGTGGG others(267): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0201 others(1): Show |
12 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108584 | ||||||
| chr13:113108615 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
108 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.65-2075A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108615 | |||||||
| chr13:113108624 | G | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-2066G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108624 | |||||||
| chr13:113108637 | C | CGTGGGTG others(10): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2044_65-2028dup others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108637 | ||||||
| chr13:113108649 | GGGAGTGT others(180): Show |
G | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2038_65-1852del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108649 | ||||||
| chr13:113108652 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-2038A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108652 | |||||||
| chr13:113108654 | TGTGGGTG others(214): Show |
T | 1 | a0001c0001t0001g0040 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-2035_65-1815del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108654 | |||||||
| chr13:113108752 | A | G | 2 | a0001c0001t0012g0061 a0001c0001t0012g0062 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.65-1938A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108752 | |||||||
| chr13:113108759 | AGGGTGTC others(78): Show |
A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.65-1907_65-1823del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108759 | ||||||
| chr13:113108768 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.65-1922C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108768 | |||||||
| chr13:113108768 | CGGGAGTG others(11): Show |
C | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1918_65-1901del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108768 | ||||||
| chr13:113108769 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-1921G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108769 | |||||||
| chr13:113108776 | T | TGGGTGTT others(10): Show |
1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1908_65-1907ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108776 | ||||||
| chr13:113108786 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1904A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108786 | |||||||
| chr13:113108789 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1901G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108789 | |||||||
| chr13:113108790 | G | T | 1 | a0001c0001t0001g0007 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.65-1900G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108790 | |||||||
| chr13:113108796 | G | T | 1 | a0002c0002t0003g0058 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.65-1894G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108796 | |||||||
| chr13:113108800 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1890C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108800 | |||||||
| chr13:113108805 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1885G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108805 | |||||||
| chr13:113108810 | T | A | 2 | a0001c0001t0001g0166 a0001c0001t0004g0194 |
2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1880T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108810 | |||||||
| chr13:113108825 | TGTGGGTG others(10): Show |
T | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1850_65-1834del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108825 | ||||||
| chr13:113108834 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1856C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108834 | |||||||
| chr13:113108839 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1851G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108839 | |||||||
| chr13:113108841 | G | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1849G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108841 | |||||||
| chr13:113108842 | A | C | 2 | a0001c0001t0001g0166 a0002c0010t0015g0084 |
2 | HG01496.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1848A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108842 | |||||||
| chr13:113108844 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1846T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108844 | |||||||
| chr13:113108861 | TGGGTGTT others(197): Show |
T | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1822_65-1619del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108861 | ||||||
| chr13:113108878 | A | T | 1 | a0001c0001t0001g0040 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-1812A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108878 | |||||||
| chr13:113108895 | TGGGTGTT others(163): Show |
T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0047 others(4): Show |
14 | HG01975.hp2 HG02015.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-1788_65-1619del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108895 | ||||||
| chr13:113108902 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0074 a0001c0001t0001g0075 |
4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1788T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108902 | |||||||
| chr13:113108905 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1785G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108905 | |||||||
| chr13:113108912 | AGGGTGTC others(78): Show |
A | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1763_65-1679del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108912 | ||||||
| chr13:113108925 | A | AGTGTGGG others(10): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0201 others(1): Show |
12 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-1764_65-1763ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108925 | ||||||
| chr13:113108927 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.65-1763C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108927 | |||||||
| chr13:113108929 | TGGGTGTC others(129): Show |
T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(39): Show |
85 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.65-1748_65-1613del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108929 | ||||||
| chr13:113108936 | CCCGGGGG others(128): Show |
C | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.65-1751_65-1617del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108936 | ||||||
| chr13:113108939 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1751G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108939 | |||||||
| chr13:113108944 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1746C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108944 | |||||||
| chr13:113108959 | AGCGTGGG others(10): Show |
A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1729_65-1713del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108959 | ||||||
| chr13:113108964 | G | A | 32 | a0001c0001t0001g0050 a0001c0001t0012g0061 a0001c0001t0012g0062 others(29): Show |
35 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-1726G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108964 | |||||||
| chr13:113108964 | G | GGGTGTCC others(214): Show |
1 | a0001c0001t0005g0103 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-1657_65-1656ins others(221): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108964 | ||||||
| chr13:113108973 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0016g0200 a0001c0003t0014g0102 |
6 | HG00140.hp1 HG00738.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-1717A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108973 | |||||||
| chr13:113108978 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(3): Show |
8 | HG00558.hp2 NA18612.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-1712T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108978 | |||||||
| chr13:113109034 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.65-1656A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109034 | |||||||
| chr13:113109034 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-1656A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109034 | |||||||
| chr13:113109123 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.65-1567C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109123 | |||||||
| chr13:113109124 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1566C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109124 | |||||||
| chr13:113109128 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.65-1562G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109128 | |||||||
| chr13:113109133 | T | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.65-1557T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109133 | |||||||
| chr13:113109236 | G | T | 1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.65-1454G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109236 | |||||||
| chr13:113109269 | G | A | 1 | a0001c0001t0019g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.65-1421G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109269 | |||||||
| chr13:113109416 | A | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-1274A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109416 | |||||||
| chr13:113109474 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.65-1216A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109474 | |||||||
| chr13:113109519 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0004g0022 |
4 | HG02886.hp1 NA18960.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1171C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109519 | |||||||
| chr13:113109612 | G | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.65-1078G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109612 | |||||||
| chr13:113109652 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.65-1038G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109652 | |||||||
| chr13:113109771 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-919A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109771 | |||||||
| chr13:113109833 | G | C | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-857G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109833 | |||||||
| chr13:113109943 | G | C | 1 | a0001c0001t0004g0021 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.65-747G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109943 | |||||||
| chr13:113110081 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.65-609G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110081 | |||||||
| chr13:113110154 | C | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0128 a0001c0001t0004g0194 |
4 | HG02145.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-536C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110154 | |||||||
| chr13:113110275 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.65-415T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110275 | |||||||
| chr13:113110296 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.65-394T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110296 | |||||||
| chr13:113110347 | CG | C | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-339delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113110347 | ||||||
| chr13:113110435 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.65-255C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110435 | |||||||
| chr13:113110510 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-180G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110510 | |||||||
| chr13:113110871 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0047 others(6): Show |
16 | HG01975.hp2 HG02015.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.225+21C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113110871 | |||||||
| chr13:113110921 | G | A | 29 | a0001c0001t0001g0050 a0001c0001t0001g0122 a0001c0001t0012g0061 others(26): Show |
32 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.225+71G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113110921 | |||||||
| chr13:113111039 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.225+189A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111039 | |||||||
| chr13:113111061 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225+211C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111061 | |||||||
| chr13:113111321 | G | GCTCACGG others(97): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0070 |
10 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+563_225+564ins others(104): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | ||||||
| chr13:113111321 | G | GCTCACGG others(167): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.225+542_225+543ins others(174): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | ||||||
| chr13:113111321 | GCTCACGG others(115): Show |
G | 5 | a0001c0001t0001g0034 a0001c0001t0016g0200 a0001c0001t0025g0034 others(2): Show |
6 | HG00280.hp2 HG02135.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+665_225+786del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | ||||||
| chr13:113111373 | A | AGGGCACA others(181): Show |
1 | a0001c0001t0001g0031 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.225+664_225+665ins others(188): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111373 | ||||||
| chr13:113111393 | A | G | 6 | a0001c0001t0001g0162 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
8 | HG01496.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+543A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111393 | |||||||
| chr13:113111396 | TCACCTCA others(11): Show |
T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
70 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.225+564_225+581del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111396 | ||||||
| chr13:113111403 | ACACTCAC others(119): Show |
A | 1 | a0001c0001t0004g0021 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+557_225+682del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111403 | ||||||
| chr13:113111425 | TCACAGGG others(417): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+615_225+1038de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111425 | ||||||
| chr13:113111480 | GAGGACAC others(233): Show |
G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(46): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.225+665_225+904del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111480 | ||||||
| chr13:113111513 | A | ACGGGTCA others(57): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+664_225+665ins others(64): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111513 | ||||||
| chr13:113111515 | A | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+665A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111515 | |||||||
| chr13:113111529 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+679T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111529 | |||||||
| chr13:113111539 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+689C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111539 | |||||||
| chr13:113111547 | T | TCACAGGG others(45): Show |
1 | a0001c0001t0005g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.225+736_225+737ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111547 | ||||||
| chr13:113111547 | T | TCACAGGG others(43): Show |
1 | a0001c0001t0005g0013 | 3 | HG02572.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.225+736_225+737ins others(50): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111547 | ||||||
| chr13:113111602 | G | GAGGACAC others(111): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0126 |
3 | HG01256.hp2 HG01258.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.225+937_225+1054du others(119): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111602 | ||||||
| chr13:113111602 | GAGGACAC others(111): Show |
G | 1 | a0001c0001t0002g0002 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.225+937_225+1054de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111602 | ||||||
| chr13:113111667 | ACAAGACA others(1): Show |
A | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+819_225+826del others(8): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111667 | ||||||
| chr13:113111681 | ACG | A | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+832_225+833del others(2): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111681 | |||||||
| chr13:113111682 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+832C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111682 | |||||||
| chr13:113111703 | A | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+853A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111703 | |||||||
| chr13:113111717 | C | T | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+867C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111717 | |||||||
| chr13:113111718 | C | CCAAGATC others(7): Show |
2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+868_225+869ins others(14): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111718 | |||||||
| chr13:113111720 | C | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+870C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111720 | |||||||
| chr13:113111731 | A | ACACT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+884_225+885ins others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111731 | ||||||
| chr13:113111733 | ACAGGGCA others(107): Show |
A | 2 | a0001c0001t0001g0191 a0001c0001t0004g0021 |
3 | HG01975.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+886_225+999del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111733 | ||||||
| chr13:113111751 | T | TCACGGGT others(56): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+920_225+921ins others(63): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111751 | ||||||
| chr13:113111765 | ACACT | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0076 |
3 | HG02451.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.225+919_225+922del others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111765 | ||||||
| chr13:113111800 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+950C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111800 | |||||||
| chr13:113111838 | C | CAGGACAC others(63): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1002_225+1003i others(72): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111838 | ||||||
| chr13:113111838 | C | CAGGACAC others(247): Show |
1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.225+1002_225+1003i others(256): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111838 | ||||||
| chr13:113111849 | A | ACACT | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.225+1002_225+1003i others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111849 | ||||||
| chr13:113111849 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0004g0021 |
3 | HG01975.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+999A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111849 | |||||||
| chr13:113111869 | T | G | 1 | a0001c0001t0004g0022 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.225+1019T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111869 | |||||||
| chr13:113111872 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1022C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111872 | |||||||
| chr13:113111912 | G | A | 2 | a0001c0001t0006g0029 a0001c0001t0006g0080 |
3 | HG00140.hp2 HG00323.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.225+1062G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111912 | |||||||
| chr13:113112039 | C | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.225+1189C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112039 | |||||||
| chr13:113112079 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0004g0021 a0001c0001t0004g0022 |
5 | HG02886.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1229G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112079 | |||||||
| chr13:113112136 | ACACT | A | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+1290_225+1293d others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112136 | ||||||
| chr13:113112205 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1355C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112205 | |||||||
| chr13:113112281 | A | C | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.225+1431A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112281 | |||||||
| chr13:113112318 | CCT | C | 2 | a0001c0001t0005g0013 a0001c0001t0005g0069 |
4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-1432_226-1431d others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112318 | ||||||
| chr13:113112339 | TACTCTCA others(11): Show |
T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-1392_226-1375d others(20): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112339 | ||||||
| chr13:113112357 | C | CACTCTCA others(484): Show |
1 | a0001c0001t0001g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.226-1200_226-710du others(492): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112357 | ||||||
| chr13:113112357 | CACTCTCA others(484): Show |
C | 2 | a0001c0001t0004g0108 a0002c0002t0003g0059 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.226-1200_226-710de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112357 | ||||||
| chr13:113112458 | A | C | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-1294A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112458 | |||||||
| chr13:113112505 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(3): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-1247A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112505 | |||||||
| chr13:113112574 | GAGGTCAC others(57): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.226-1131_226-1068d others(66): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112574 | ||||||
| chr13:113112710 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-1042C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112710 | |||||||
| chr13:113112713 | A | ACACT | 68 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.226-1036_226-1035i others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112713 | ||||||
| chr13:113112749 | A | G | 1 | a0001c0001t0004g0022 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.226-1003A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112749 | |||||||
| chr13:113112828 | C | A | 3 | a0001c0001t0006g0029 a0001c0001t0006g0080 a0001c0001t0006g0081 |
4 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-924C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112828 | |||||||
| chr13:113112848 | T | TACTCTCA others(11): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0130 others(4): Show |
15 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-901_226-884dup others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112848 | ||||||
| chr13:113112922 | A | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(3): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-830A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112922 | |||||||
| chr13:113112984 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.226-768G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112984 | |||||||
| chr13:113113022 | C | T | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226-730C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113022 | |||||||
| chr13:113113049 | C | CATT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(3): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-701_226-700ins others(3): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113113049 | ||||||
| chr13:113113068 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.226-684G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113068 | |||||||
| chr13:113113080 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.226-672A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113080 | |||||||
| chr13:113113114 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(3): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-638C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113114 | |||||||
| chr13:113113130 | A | T | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-622A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113130 | |||||||
| chr13:113113209 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-543T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113209 | |||||||
| chr13:113113348 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.226-404C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113348 | |||||||
| chr13:113113392 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(2): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-360T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113392 | |||||||
| chr13:113113518 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-234T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113518 | |||||||
| chr13:113113519 | G | T | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-233G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113519 | |||||||
| chr13:113113520 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.226-232T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113520 | |||||||
| chr13:113113520 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-232T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113520 | |||||||
| chr13:113113584 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.226-168G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113584 | |||||||
| chr13:113113641 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18960.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.226-111G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113641 | |||||||
| chr13:113114173 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.364+213C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114173 | |||||||
| chr13:113114217 | G | A | 1 | a0002c0002t0003g0058 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.364+257G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114217 | |||||||
| chr13:113114271 | C | T | 2 | a0001c0001t0005g0013 a0001c0001t0016g0200 |
4 | HG02572.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+311C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114271 | |||||||
| chr13:113114279 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364+319C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114279 | |||||||
| chr13:113114324 | AG | A | 35 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(32): Show |
43 | HG01515.hp2 HG01517.hp2 HG02040.hp1 others(40): Show |
intron_variant | MODIFIER | c.364+368delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113114324 | ||||||
| chr13:113114327 | GGT | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(22): Show |
39 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.364+368_364+369del others(2): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114327 | |||||||
| chr13:113114328 | G | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0004g0178 others(6): Show |
12 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+368G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114328 | |||||||
| chr13:113114331 | TG | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.364+372delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114331 | |||||||
| chr13:113114332 | G | GT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(10): Show |
21 | HG00423.hp2 HG01975.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.364+382dupT | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113114332 | ||||||
| chr13:113114332 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(64): Show |
93 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.364+372G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114332 | |||||||
| chr13:113114445 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.364+485C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114445 | |||||||
| chr13:113114457 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.364+497G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114457 | |||||||
| chr13:113114577 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.364+617G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114577 | |||||||
| chr13:113114888 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0157 a0001c0001t0001g0189 |
7 | NA18944.hp1 NA18956.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-772T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114888 | |||||||
| chr13:113114912 | A | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0004g0022 others(3): Show |
8 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-748A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114912 | |||||||
| chr13:113115032 | G | C | 37 | a0001c0003t0001g0051 a0001c0003t0001g0054 a0001c0003t0014g0077 others(34): Show |
40 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.365-628G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115032 | |||||||
| chr13:113115114 | C | T | 1 | a0002c0002t0003g0025 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365-546C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115114 | |||||||
| chr13:113115159 | G | A | 1 | a0002c0002t0003g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.365-501G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115159 | |||||||
| chr13:113115219 | C | T | 2 | a0001c0001t0012g0061 a0001c0001t0012g0062 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.365-441C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115219 | |||||||
| chr13:113115325 | T | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0162 others(44): Show |
60 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.365-335T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115325 | |||||||
| chr13:113115362 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.365-298C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115362 | |||||||
| chr13:113115599 | G | A | 1 | a0001c0001t0012g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.365-61G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115599 | |||||||
| chr13:113115603 | G | A | 33 | a0001c0003t0001g0051 a0001c0003t0001g0054 a0001c0003t0014g0077 others(30): Show |
36 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.365-57G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115603 | |||||||
| chr13:113115613 | G | A | 1 | a0002c0002t0008g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.365-47G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115613 | |||||||
| chr13:113115849 | A | C | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.505+49A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113115849 | |||||||
| chr13:113115971 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.505+171G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113115971 | |||||||
| chr13:113116038 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.505+238G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116038 | |||||||
| chr13:113116046 | G | A | 1 | a0001c0001t0017g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.505+246G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116046 | |||||||
| chr13:113116173 | G | A | 1 | a0002c0010t0015g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.505+373G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116173 | |||||||
| chr13:113116207 | A | C | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.505+407A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116207 | |||||||
| chr13:113116316 | C | T | 1 | a0001c0001t0001g0045 | 2 | NA18993.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.506-450C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116316 | |||||||
| chr13:113116337 | C | T | 1 | a0001c0001t0016g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.506-429C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116337 | |||||||
| chr13:113116348 | A | G | 1 | a0002c0002t0003g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.506-418A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116348 | |||||||
| chr13:113116355 | T | C | 3 | a0001c0001t0012g0061 a0001c0001t0012g0062 a0001c0001t0017g0177 |
3 | HG02559.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.506-411T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116355 | |||||||
| chr13:113116358 | T | C | 1 | a0003c0008t0002g0133 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.506-408T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116358 | |||||||
| chr13:113116389 | A | C | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-377A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116389 | |||||||
| chr13:113116562 | G | A | 35 | a0001c0001t0004g0022 a0001c0001t0016g0200 a0001c0001t0023g0164 others(32): Show |
40 | HG00673.hp1 HG01243.hp2 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.506-204G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116562 | |||||||
| chr13:113116592 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.506-174C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116592 | |||||||
| chr13:113116683 | A | T | 1 | a0002c0002t0003g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.506-83A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116683 | |||||||
| chr13:113116716 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.506-50C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116716 | |||||||
| chr13:113116754 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-12T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116754 | |||||||
| chr13:113116755 | G | T | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-11G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116755 | |||||||
| chr13:113116756 | T | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-10T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116756 | |||||||
| chr13:113116956 | A | G | 1 | a0006c0011t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.615+81A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113116956 | |||||||
| chr13:113117132 | C | T | 2 | a0001c0001t0012g0061 a0001c0001t0012g0062 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.615+257C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113117132 | |||||||
| chr13:113117365 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.616-108G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113117365 | |||||||
| chr13:113117585 | TCGCGGTG others(30): Show |
T | 1 | a0003c0008t0002g0133 | 1 | HG01975.hp1 | splice_region_variant&intron_variant | LOW | c.739+7_739+43delACC others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117585 | ||||||
| chr13:113117603 | A | ACCACTCT others(30): Show |
80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(77): Show |
130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.739+15_739+51dupCC others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | ||||||
| chr13:113117603 | A | ACCACTCT others(67): Show |
4 | a0001c0001t0005g0013 a0001c0001t0005g0069 a0001c0001t0005g0103 others(1): Show |
6 | HG01891.hp2 HG01952.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+51_739+52insCC others(72): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | ||||||
| chr13:113117603 | A | ACCACTCT others(29): Show |
1 | a0001c0001t0001g0004 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.739+30_739+31insTG others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | ||||||
| chr13:113117648 | T | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
157 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.739+52T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117648 | |||||||
| chr13:113117648 | TCCCTGTC others(30): Show |
T | 2 | a0001c0001t0001g0033 a0001c0001t0002g0078 |
3 | HG00323.hp1 HG01070.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.739+128_739+164del others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117648 | ||||||
| chr13:113117694 | G | GACCGCGG others(30): Show |
1 | a0002c0002t0009g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.739+134_739+135ins others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117694 | ||||||
| chr13:113117724 | C | CCTGTCCG others(67): Show |
1 | a0001c0001t0017g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.739+164_739+165ins others(74): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117724 | ||||||
| chr13:113117724 | C | CCTGTCCG others(30): Show |
2 | a0001c0001t0012g0061 a0001c0001t0012g0062 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.739+155_739+191dup others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117724 | ||||||
| chr13:113117734 | C | CGCGGTGC others(30): Show |
1 | a0001c0003t0010g0042 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.739+164_739+165ins others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117734 | ||||||
| chr13:113117761 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0083 a0001c0001t0002g0089 others(1): Show |
5 | NA18952.hp2 NA18956.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.739+165G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117761 | |||||||
| chr13:113117773 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.739+177C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117773 | |||||||
| chr13:113117996 | C | G | 1 | a0001c0001t0013g0038 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.739+400C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117996 | |||||||
| chr13:113117999 | G | A | 1 | a0001c0001t0017g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.739+403G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117999 | |||||||
| chr13:113118028 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.740-385C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118028 | |||||||
| chr13:113118086 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.740-327G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118086 | |||||||
| chr13:113118136 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.740-277G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118136 | |||||||
| chr13:113118253 | G | T | 1 | a0002c0002t0003g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.740-160G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118253 | |||||||
| chr13:113118326 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.740-87C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118326 | |||||||
| chr13:113118393 | G | A | 34 | a0002c0002t0001g0024 a0002c0002t0003g0012 a0002c0002t0003g0024 others(31): Show |
37 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.740-20G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118393 |