Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79034 |
| ensemblid | ENSG00000146576.13 |
| hgncid | 21702 |
| symbol | INTS15 |
| name | integrator complex subunit 15 |
| refseq_nuc | NM_024067.4 |
| refseq_prot | NP_076972.2 |
| ensembl_nuc | ENST00000344417.10 |
| ensembl_prot | ENSP00000340220.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 6590021 |
| end | 6608726 |
| strand | + |
| ver | v1.2 |
| region | chr7:6590021-6608726 |
| region5000 | chr7:6585021-6613726 |
| regionname0 | INTS15_chr7_6590021_6608726 |
| regionname5000 | INTS15_chr7_6585021_6613726 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 449 | 387 | 89 | 76 | 161 | 16 | 43 | 120 | INTS15_chr7_6585021_6613726 | INTS15 | MSDIR others(444): Show |
chr7 | 6585021 | 6613726 |
| a0002 | 0/0 | 449 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | MSDIR others(444): Show |
chr7 | 6585021 | 6613726 |
| a0003 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | MSDIR others(444): Show |
chr7 | 6585021 | 6613726 |
| a0004 | 0/0 | 449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | MSDIR others(444): Show |
chr7 | 6585021 | 6613726 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1347 | 262 | 79 | 55 | 95 | 11 | 22 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0001c0002 | 1/0 | 1347 | 101 | 4 | 8 | 65 | 3 | 20 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0001c0003 | 0/1 | 1347 | 16 | 1 | 11 | 0 | 2 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0001c0005 | 0/0 | 1347 | 4 | 2 | 2 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0001c0006 | 0/0 | 1347 | 3 | 3 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0001c0007 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0002c0004 | 0/0 | 1347 | 5 | 5 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0003c0008 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 | ||
| a0004c0009 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | ATGAG others(1342): Show |
chr7 | 6585021 | 6613726 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2178 | 258 | 78 | 52 | 95 | 11 | 22 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0001t0002 | 0/0 | 2178 | 3 | 0 | 3 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0001t0004 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0002t0001 | 1/0 | 2178 | 98 | 4 | 8 | 64 | 1 | 20 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0002t0003 | 0/0 | 2178 | 2 | 0 | 0 | 0 | 2 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0002t0006 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0003t0001 | 0/1 | 2178 | 16 | 1 | 11 | 0 | 2 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0005t0001 | 0/0 | 2178 | 4 | 2 | 2 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0006t0001 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0001c0007t0005 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0002c0004t0001 | 0/0 | 2178 | 5 | 5 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0003c0008t0001 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| a0004c0009t0001 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | ATTCG others(2173): Show |
chr7 | 6585021 | 6613726 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 5 | 4 | 16 | 1 | 4 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0003 | 0/0 | 9 | 1 | 1 | 2 | 5 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 2 | 6 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0009 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0002 | 0/0 | 11 | 0 | 0 | 9 | 1 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0002t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0005t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0005t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0001c0007t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0002c0004t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0002c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0003c0008t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| a0004c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0028 | EUR | FIN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00558 | hp1 | a0003 | c0008 | t0001 | g0111 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0265 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0267 | AMR | PUR | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0209 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0035 | EUR | IBS | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02056 | hp2 | a0001 | c0007 | t0005 | g0042 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0014 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0263 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0269 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0264 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0085 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0266 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0014 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03654 | hp2 | a0004 | c0009 | t0001 | g0011 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0078 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0218 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | BEB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | STU | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0268 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18945 | hp2 | a0001 | c0002 | t0006 | g0011 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19240 | hp1 | a0002 | c0004 | t0001 | g0089 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ASW | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0080 | EUR | TSI | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | GIH | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02109 | hp2 | a0002 | c0004 | t0001 | g0014 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | USA | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0082 | REF | REF | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0167 | REF | REF | INTS15_chr7_6585021_6613726 | INTS15 | chr7 | 6585021 | 6613726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:6590452 | A | G | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.169A>G | p.Lys57Glu | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/6 | 432/2178 | 169/1350 | 57/449 | chr7 | 6590452 | |||
| chr7:6599981 | C | T | 1 | a0002 | 5 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
missense_variant | MODERATE | c.733C>T | p.Arg245Cys | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/6 | 996/2178 | 733/1350 | 245/449 | chr7 | 6599981 | |||
| chr7:6600333 | C | T | 1 | a0003 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1085C>T | p.Ser362Leu | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/6 | 1348/2178 | 1085/1350 | 362/449 | chr7 | 6600333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:6590472 | C | T | 1 | a0001c0006 | 3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.189C>T | p.Pro63Pro | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/6 | 452/2178 | 189/1350 | 63/449 | chr7 | 6590472 | |||
| chr7:6591783 | G | T | 1 | a0001c0005 | 4 | HG01175.hp1 HG01243.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.330G>T | p.Arg110Arg | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/6 | 593/2178 | 330/1350 | 110/449 | chr7 | 6591783 | |||
| chr7:6599965 | G | A | 1 | a0001c0007 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.717G>A | p.Pro239Pro | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/6 | 980/2178 | 717/1350 | 239/449 | chr7 | 6599965 | |||
| chr7:6600322 | G | A | 1 | a0001c0003 | 15 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
synonymous_variant | LOW | c.1074G>A | p.Val358Val | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/6 | 1337/2178 | 1074/1350 | 358/449 | chr7 | 6600322 | |||
| chr7:6608107 | T | C | 7 | a0001c0001 a0001c0003 a0001c0005 others(4): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
synonymous_variant | LOW | c.1296T>C | p.His432His | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 6/6 | 1559/2178 | 1296/1350 | 432/449 | chr7 | 6608107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:6590045 | G | A | 1 | a0001c0001t0004 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-239G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/6 | 239 | chr7 | 6590045 | ||||||
| chr7:6590186 | C | T | 1 | a0001c0002t0006 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/6 | 98 | chr7 | 6590186 | ||||||
| chr7:6608327 | A | T | 1 | a0001c0001t0002 | 3 | HG01099.hp2 HG02004.hp1 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*166A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 6/6 | 166 | chr7 | 6608327 | ||||||
| chr7:6608614 | C | G | 1 | a0001c0002t0003 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 6/6 | 453 | chr7 | 6608614 | ||||||
| chr7:6608715 | T | G | 1 | a0001c0007t0005 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*554T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 6/6 | 554 | chr7 | 6608715 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:6590503 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG03130.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+28G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590503 | |||||||
| chr7:6590813 | A | C | 1 | a0001c0005t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+338A>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590813 | |||||||
| chr7:6590878 | G | A | 1 | a0001c0007t0005g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.192+403G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590878 | |||||||
| chr7:6590879 | C | T | 1 | a0001c0006t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192+404C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590879 | |||||||
| chr7:6590914 | C | G | 4 | a0001c0005t0001g0265 a0001c0005t0001g0266 a0001c0005t0001g0267 others(1): Show |
4 | HG01175.hp1 HG01243.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+439C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590914 | |||||||
| chr7:6590928 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.192+453T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590928 | |||||||
| chr7:6590952 | C | T | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.192+477C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590952 | |||||||
| chr7:6590992 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+517C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6590992 | |||||||
| chr7:6591078 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG03130.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-568T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591078 | |||||||
| chr7:6591157 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-489C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591157 | |||||||
| chr7:6591228 | C | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193-418C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591228 | |||||||
| chr7:6591268 | CT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
142 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.193-361delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 6591268 | ||||||
| chr7:6591352 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-294C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591352 | |||||||
| chr7:6591368 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.193-278G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591368 | |||||||
| chr7:6591369 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.193-277C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591369 | |||||||
| chr7:6591426 | C | CT | 19 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(16): Show |
24 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-220_193-219ins others(1): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591426 | |||||||
| chr7:6591426 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.193-220C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591426 | |||||||
| chr7:6591593 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
6 | HG02723.hp1 HG03453.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-53A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 1/5 | chr7 | 6591593 | |||||||
| chr7:6591877 | A | G | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02572.hp2 HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.414+10A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6591877 | |||||||
| chr7:6591901 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.414+34G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6591901 | |||||||
| chr7:6591912 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+45C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6591912 | |||||||
| chr7:6591946 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414+79C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6591946 | |||||||
| chr7:6591962 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.414+95A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6591962 | |||||||
| chr7:6592028 | G | A | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.414+161G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592028 | |||||||
| chr7:6592059 | T | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02965.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.414+192T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592059 | |||||||
| chr7:6592172 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.414+305A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592172 | |||||||
| chr7:6592207 | T | G | 19 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(16): Show |
24 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.414+340T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592207 | |||||||
| chr7:6592253 | T | G | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.414+386T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592253 | |||||||
| chr7:6592313 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.414+446C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592313 | |||||||
| chr7:6592335 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.414+468G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592335 | |||||||
| chr7:6592336 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.414+469G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592336 | |||||||
| chr7:6592428 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.414+561G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592428 | |||||||
| chr7:6592544 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414+677G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592544 | |||||||
| chr7:6592566 | C | CA | 9 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG02647.hp1 NA18946.hp2 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+709dupA | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6592566 | ||||||
| chr7:6592650 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.414+783C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592650 | |||||||
| chr7:6592689 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+822G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592689 | |||||||
| chr7:6592777 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+910T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592777 | |||||||
| chr7:6592822 | C | G | 1 | a0001c0007t0005g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.414+955C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592822 | |||||||
| chr7:6592847 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG00639.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.414+980C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592847 | |||||||
| chr7:6592990 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(66): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.414+1123C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6592990 | |||||||
| chr7:6593008 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(8): Show |
15 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+1141A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593008 | |||||||
| chr7:6593113 | C | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
5 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+1246C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593113 | |||||||
| chr7:6593141 | A | T | 2 | a0001c0002t0001g0247 a0001c0002t0001g0248 |
2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.414+1274A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593141 | |||||||
| chr7:6593191 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.415-1244C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593191 | |||||||
| chr7:6593224 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.415-1211T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593224 | |||||||
| chr7:6593286 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-1149G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593286 | |||||||
| chr7:6593289 | A | G | 1 | a0001c0003t0001g0029 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.415-1146A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593289 | |||||||
| chr7:6593329 | G | GT | 50 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0038 others(47): Show |
55 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.415-1087dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6593329 | ||||||
| chr7:6593329 | G | GTT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(21): Show |
33 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.415-1088_415-1087d others(4): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6593329 | ||||||
| chr7:6593329 | G | GTTT | 9 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0106 others(6): Show |
9 | HG02055.hp1 HG02258.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-1089_415-1087d others(5): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6593329 | ||||||
| chr7:6593363 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.415-1072C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593363 | |||||||
| chr7:6593455 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.415-980C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593455 | |||||||
| chr7:6593475 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(28): Show |
40 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.415-960C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593475 | |||||||
| chr7:6593524 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.415-911C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593524 | |||||||
| chr7:6593526 | G | T | 8 | a0001c0003t0001g0006 a0001c0003t0001g0028 a0001c0003t0001g0029 others(5): Show |
15 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-909G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593526 | |||||||
| chr7:6593535 | T | C | 19 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(16): Show |
24 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.415-900T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593535 | |||||||
| chr7:6593555 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
7 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-880C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593555 | |||||||
| chr7:6593572 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-863G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593572 | |||||||
| chr7:6593628 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0092 a0001c0001t0001g0094 |
4 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-807C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593628 | |||||||
| chr7:6593629 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.415-806C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593629 | |||||||
| chr7:6593642 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(66): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.415-793T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593642 | |||||||
| chr7:6593649 | G | GT | 8 | a0001c0001t0001g0197 a0001c0001t0001g0243 a0001c0001t0001g0244 others(5): Show |
8 | HG02738.hp2 HG03130.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-769dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6593649 | ||||||
| chr7:6593649 | GT | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(79): Show |
138 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.415-769delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6593649 | ||||||
| chr7:6593735 | A | C | 1 | a0001c0002t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.415-700A>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593735 | |||||||
| chr7:6593736 | C | G | 1 | a0001c0002t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.415-699C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593736 | |||||||
| chr7:6593761 | C | T | 1 | a0001c0005t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415-674C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593761 | |||||||
| chr7:6593940 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.415-495C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593940 | |||||||
| chr7:6593953 | G | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(8): Show |
15 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-482G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593953 | |||||||
| chr7:6593960 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-475A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593960 | |||||||
| chr7:6593992 | AG | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.415-442delG | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593992 | |||||||
| chr7:6593996 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.415-439T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593996 | |||||||
| chr7:6593998 | T | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.415-437T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6593998 | |||||||
| chr7:6594001 | C | CT | 44 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
60 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.415-410dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6594001 | ||||||
| chr7:6594001 | C | CTT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(62): Show |
115 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.415-411_415-410dup others(2): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6594001 | ||||||
| chr7:6594001 | C | CTTT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0051 others(10): Show |
15 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-412_415-410dup others(3): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6594001 | ||||||
| chr7:6594001 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.415-434C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594001 | |||||||
| chr7:6594001 | CT | C | 11 | a0001c0001t0001g0107 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
12 | HG01167.hp2 HG01256.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-410delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 6594001 | ||||||
| chr7:6594053 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(85): Show |
147 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.415-382C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594053 | |||||||
| chr7:6594196 | C | G | 1 | a0001c0002t0001g0189 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.415-239C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594196 | |||||||
| chr7:6594198 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-237A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594198 | |||||||
| chr7:6594268 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG02723.hp1 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-167A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594268 | |||||||
| chr7:6594301 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.415-134C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594301 | |||||||
| chr7:6594427 | C | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
6 | HG02723.hp1 HG03453.hp2 HG03540.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.415-8C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 2/5 | chr7 | 6594427 | |||||||
| chr7:6594695 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.580+95C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594695 | |||||||
| chr7:6594702 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+102T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594702 | |||||||
| chr7:6594772 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580+172G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594772 | |||||||
| chr7:6594784 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.580+184T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594784 | |||||||
| chr7:6594801 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.580+201A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594801 | |||||||
| chr7:6594996 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.580+396A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6594996 | |||||||
| chr7:6595023 | C | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG01243.hp1 HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.580+423C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595023 | |||||||
| chr7:6595157 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.580+557G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595157 | |||||||
| chr7:6595157 | G | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.580+557G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595157 | |||||||
| chr7:6595220 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.580+620C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595220 | |||||||
| chr7:6595221 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.580+621A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595221 | |||||||
| chr7:6595277 | C | G | 1 | a0001c0007t0005g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.580+677C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595277 | |||||||
| chr7:6595295 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.580+695C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595295 | |||||||
| chr7:6595300 | C | T | 1 | a0001c0007t0005g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.580+700C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595300 | |||||||
| chr7:6595330 | T | G | 1 | a0001c0002t0001g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.580+730T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595330 | |||||||
| chr7:6595363 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+763T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595363 | |||||||
| chr7:6595390 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580+790C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595390 | |||||||
| chr7:6595392 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0074 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.580+792G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595392 | |||||||
| chr7:6595431 | C | T | 1 | a0001c0007t0005g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.580+831C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595431 | |||||||
| chr7:6595433 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.580+833G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595433 | |||||||
| chr7:6595534 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.580+934G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595534 | |||||||
| chr7:6595567 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG03130.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+967G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595567 | |||||||
| chr7:6595572 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580+972A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595572 | |||||||
| chr7:6595609 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+1009A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595609 | |||||||
| chr7:6595629 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.580+1029C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595629 | |||||||
| chr7:6595655 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+1055C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595655 | |||||||
| chr7:6595820 | C | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.580+1220C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595820 | |||||||
| chr7:6595925 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.580+1325A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595925 | |||||||
| chr7:6595942 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.580+1342C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595942 | |||||||
| chr7:6595958 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+1358T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595958 | |||||||
| chr7:6595964 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.580+1364C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595964 | |||||||
| chr7:6595969 | T | G | 1 | a0002c0004t0001g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.580+1369T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6595969 | |||||||
| chr7:6596050 | C | CT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.580+1461dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6596050 | ||||||
| chr7:6596161 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0149 others(1): Show |
7 | HG01192.hp2 HG01515.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+1561C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596161 | |||||||
| chr7:6596169 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0208 |
2 | HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.580+1569A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596169 | |||||||
| chr7:6596201 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580+1601G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596201 | |||||||
| chr7:6596263 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.580+1663C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596263 | |||||||
| chr7:6596298 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.580+1698C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596298 | |||||||
| chr7:6596318 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.580+1718T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596318 | |||||||
| chr7:6596376 | C | CT | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.580+1796dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6596376 | ||||||
| chr7:6596376 | CT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0084 others(6): Show |
12 | HG00323.hp1 HG01070.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.580+1796delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6596376 | ||||||
| chr7:6596427 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.580+1827G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596427 | |||||||
| chr7:6596430 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.580+1830G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596430 | |||||||
| chr7:6596463 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.580+1863C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596463 | |||||||
| chr7:6596495 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580+1895C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596495 | |||||||
| chr7:6596531 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+1931A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596531 | |||||||
| chr7:6596539 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580+1939C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596539 | |||||||
| chr7:6596682 | T | G | 1 | a0001c0002t0001g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.580+2082T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596682 | |||||||
| chr7:6596814 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0129 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.580+2214G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6596814 | |||||||
| chr7:6597024 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580+2424C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597024 | |||||||
| chr7:6597120 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+2520C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597120 | |||||||
| chr7:6597157 | G | C | 1 | a0001c0002t0001g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.580+2557G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597157 | |||||||
| chr7:6597200 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(7): Show |
14 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.580+2600C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597200 | |||||||
| chr7:6597299 | G | GT | 9 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00621.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.581-2517dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6597299 | ||||||
| chr7:6597332 | T | C | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.581-2497T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597332 | |||||||
| chr7:6597363 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.581-2466C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597363 | |||||||
| chr7:6597381 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.581-2448A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597381 | |||||||
| chr7:6597398 | G | A | 3 | a0001c0002t0001g0019 a0001c0002t0001g0210 a0001c0002t0001g0211 |
5 | NA18974.hp2 NA18982.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-2431G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597398 | |||||||
| chr7:6597448 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
118 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.581-2381C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597448 | |||||||
| chr7:6597479 | G | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-2350G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597479 | |||||||
| chr7:6597648 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.581-2181C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597648 | |||||||
| chr7:6597730 | C | CAG | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.581-2099_581-2098i others(4): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597730 | |||||||
| chr7:6597801 | G | A | 1 | a0001c0002t0001g0184 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.581-2028G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6597801 | |||||||
| chr7:6598020 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.581-1809G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598020 | |||||||
| chr7:6598085 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0237 others(3): Show |
7 | HG02647.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-1744C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598085 | |||||||
| chr7:6598107 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.581-1722C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598107 | |||||||
| chr7:6598185 | C | T | 1 | a0001c0002t0001g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.581-1644C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598185 | |||||||
| chr7:6598196 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.581-1633C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598196 | |||||||
| chr7:6598197 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.581-1632G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598197 | |||||||
| chr7:6598205 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.581-1624C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598205 | |||||||
| chr7:6598209 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.581-1620C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598209 | |||||||
| chr7:6598272 | C | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.581-1557C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598272 | |||||||
| chr7:6598361 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.581-1468C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598361 | |||||||
| chr7:6598387 | T | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(62): Show |
119 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.581-1442T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598387 | |||||||
| chr7:6598468 | C | CA | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.581-1344dupA | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598468 | ||||||
| chr7:6598468 | C | CAA | 13 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0056 others(10): Show |
15 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.581-1345_581-1344d others(4): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598468 | ||||||
| chr7:6598512 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.581-1317G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598512 | |||||||
| chr7:6598523 | C | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.581-1306C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598523 | |||||||
| chr7:6598640 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.581-1189G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598640 | |||||||
| chr7:6598735 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.581-1094_581-1093i others(13): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598735 | |||||||
| chr7:6598735 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0002g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.581-1094_581-1093i others(15): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598735 | |||||||
| chr7:6598735 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0134 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.581-1094_581-1093i others(21): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598735 | |||||||
| chr7:6598735 | T | TTG | 32 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0130 others(29): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.581-1044_581-1043d others(4): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTG | 30 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(27): Show |
41 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.581-1046_581-1043d others(6): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTG | 15 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0127 others(12): Show |
23 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.581-1048_581-1043d others(8): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0001g0054 a0001c0001t0001g0120 a0001c0001t0001g0142 others(9): Show |
12 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-1050_581-1043d others(10): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(3): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0109 a0001c0001t0001g0116 others(5): Show |
12 | HG01975.hp2 HG01978.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-1052_581-1043d others(12): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(5): Show |
1 | a0001c0002t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.581-1054_581-1043d others(14): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0143 a0001c0001t0001g0191 a0001c0001t0001g0259 others(2): Show |
5 | HG01952.hp2 HG02572.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-1056_581-1043d others(16): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0001g0181 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.581-1060_581-1043d others(20): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0001g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.581-1062_581-1043d others(22): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | TTG | T | 8 | a0001c0001t0001g0107 a0001c0001t0001g0117 a0001c0001t0001g0135 others(5): Show |
10 | HG02602.hp1 HG03669.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.581-1044_581-1043d others(4): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | TTGTG | T | 9 | a0001c0001t0001g0201 a0001c0002t0001g0037 a0001c0002t0001g0123 others(6): Show |
10 | HG01981.hp2 HG02135.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-1046_581-1043d others(6): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0244 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.581-1054_581-1043d others(14): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598735 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0240 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.581-1056_581-1043d others(16): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598735 | ||||||
| chr7:6598752 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.581-1077T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598752 | |||||||
| chr7:6598763 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0190 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.581-1066G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598763 | |||||||
| chr7:6598764 | TGTGTGTG others(16): Show |
T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0190 a0001c0007t0005g0042 |
3 | HG02056.hp2 HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.581-1064_581-1042d others(25): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598764 | |||||||
| chr7:6598765 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-1064G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598765 | |||||||
| chr7:6598766 | TGTGTGTG others(14): Show |
T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 |
4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-1062_581-1042d others(23): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598766 | |||||||
| chr7:6598769 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0233 |
2 | HG02129.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.581-1060G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598769 | |||||||
| chr7:6598770 | TGTGTGTG others(10): Show |
T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0233 |
2 | HG02129.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.581-1058_581-1042d others(19): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598770 | |||||||
| chr7:6598771 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0228 others(4): Show |
8 | HG01928.hp1 HG01943.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-1058G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598771 | |||||||
| chr7:6598772 | TGTGTGTG others(8): Show |
T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0228 others(4): Show |
8 | HG01928.hp1 HG01943.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-1056_581-1042d others(17): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598772 | |||||||
| chr7:6598773 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0235 a0001c0001t0001g0256 |
4 | HG01070.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1056G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598773 | |||||||
| chr7:6598774 | TGTGTGTG others(6): Show |
T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0235 a0001c0001t0001g0256 |
4 | HG01070.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1054_581-1042d others(15): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598774 | |||||||
| chr7:6598775 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
5 | HG00642.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-1054G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598775 | |||||||
| chr7:6598776 | TGTGTGTG others(4): Show |
T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
5 | HG00642.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-1052_581-1042d others(13): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598776 | |||||||
| chr7:6598777 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0092 |
3 | HG01081.hp1 HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.581-1052G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598777 | |||||||
| chr7:6598778 | TGTGTGTG others(2): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0092 |
3 | HG01081.hp1 HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.581-1050_581-1042d others(11): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598778 | |||||||
| chr7:6598779 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.581-1050G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598779 | |||||||
| chr7:6598781 | G | A | 2 | a0001c0001t0001g0040 a0001c0006t0001g0268 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.581-1048G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598781 | |||||||
| chr7:6598783 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0237 others(1): Show |
4 | HG02004.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1046G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598783 | |||||||
| chr7:6598784 | TGTA | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0237 others(1): Show |
4 | HG02004.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1044_581-1042d others(5): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598784 | |||||||
| chr7:6598785 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0001g0240 others(3): Show |
6 | HG01934.hp2 HG02300.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1044G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598785 | |||||||
| chr7:6598785 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.581-1043_581-1042i others(12): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598785 | ||||||
| chr7:6598785 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.581-1043_581-1042i others(14): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598785 | ||||||
| chr7:6598785 | G | GTGTGTGT others(12): Show |
1 | a0001c0001t0001g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.581-1043_581-1042i others(21): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598785 | ||||||
| chr7:6598786 | T | TGTA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0034 others(6): Show |
9 | HG00408.hp2 HG00735.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(5): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(13): Show |
20 | HG00673.hp2 HG00738.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(7): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0024 others(17): Show |
25 | HG00323.hp1 HG01123.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(9): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(2): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0031 others(10): Show |
16 | HG00423.hp2 HG01243.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(11): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(4): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(10): Show |
15 | HG00544.hp2 HG00639.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(13): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(6): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(8): Show |
14 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(15): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(8): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(6): Show |
13 | HG00639.hp1 HG01943.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(17): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(10): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
11 | HG02155.hp1 HG03195.hp2 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(19): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(12): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(4): Show |
7 | HG01099.hp2 HG03098.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(21): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(14): Show |
1 | a0001c0001t0001g0027 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.581-1043_581-1042i others(23): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | T | TGTGTGTG others(16): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(1): Show |
4 | HG00741.hp2 HG01928.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-1043_581-1042i others(25): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598786 | TA | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0003t0001g0006 others(1): Show |
4 | HG01934.hp2 HG02300.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1042delA | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598786 | |||||||
| chr7:6598787 | A | AT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0253 others(4): Show |
8 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-1028dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 6598787 | ||||||
| chr7:6598787 | A | G | 6 | a0001c0001t0001g0145 a0001c0002t0001g0002 a0001c0002t0001g0169 others(3): Show |
6 | HG00621.hp2 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1042A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598787 | |||||||
| chr7:6598787 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
142 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.581-1042A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598787 | |||||||
| chr7:6598788 | T | A | 2 | a0001c0001t0004g0239 a0001c0007t0005g0042 |
2 | HG01891.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.581-1041T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598788 | |||||||
| chr7:6598789 | T | A | 4 | a0001c0002t0001g0169 a0001c0002t0001g0175 a0001c0002t0001g0188 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1040T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598789 | |||||||
| chr7:6598976 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.581-853C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6598976 | |||||||
| chr7:6599114 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0001t0001g0095 others(3): Show |
7 | HG02559.hp1 HG02723.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-715G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599114 | |||||||
| chr7:6599189 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.581-640C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599189 | |||||||
| chr7:6599315 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
118 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.581-514C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599315 | |||||||
| chr7:6599326 | G | T | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.581-503G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599326 | |||||||
| chr7:6599329 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-500C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599329 | |||||||
| chr7:6599331 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-498A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599331 | |||||||
| chr7:6599332 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(86): Show |
148 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.581-497A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599332 | |||||||
| chr7:6599332 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-497A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599332 | |||||||
| chr7:6599333 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-496G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599333 | |||||||
| chr7:6599334 | T | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-495T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599334 | |||||||
| chr7:6599335 | T | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-494T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599335 | |||||||
| chr7:6599338 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-491G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599338 | |||||||
| chr7:6599341 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-488T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599341 | |||||||
| chr7:6599342 | TGGGACGG others(76): Show |
T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02040.hp1 HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.581-486_581-404del others(83): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599342 | |||||||
| chr7:6599454 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.581-375G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599454 | |||||||
| chr7:6599466 | G | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
118 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.581-363G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599466 | |||||||
| chr7:6599479 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.581-350G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599479 | |||||||
| chr7:6599603 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(37): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.581-226C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599603 | |||||||
| chr7:6599605 | A | T | 1 | a0001c0005t0001g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.581-224A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599605 | |||||||
| chr7:6599778 | C | T | 3 | a0001c0002t0001g0019 a0001c0002t0001g0210 a0001c0002t0001g0211 |
5 | NA18974.hp2 NA18982.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-51C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 3/5 | chr7 | 6599778 | |||||||
| chr7:6600401 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1108+45C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600401 | |||||||
| chr7:6600447 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1108+91C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600447 | |||||||
| chr7:6600470 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1108+114C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600470 | |||||||
| chr7:6600493 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0190 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1108+137G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600493 | |||||||
| chr7:6600504 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1108+148G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600504 | |||||||
| chr7:6600519 | C | T | 1 | a0001c0005t0001g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1108+163C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600519 | |||||||
| chr7:6600604 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1108+248G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600604 | |||||||
| chr7:6600678 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0093 |
3 | HG02451.hp2 HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1108+322G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600678 | |||||||
| chr7:6600799 | A | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG03130.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108+443A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600799 | |||||||
| chr7:6600985 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1108+629A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6600985 | |||||||
| chr7:6601088 | C | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1108+732C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601088 | |||||||
| chr7:6601106 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1108+750A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601106 | |||||||
| chr7:6601113 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG03130.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108+757T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601113 | |||||||
| chr7:6601538 | C | T | 1 | a0001c0005t0001g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1109-563C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601538 | |||||||
| chr7:6601681 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0190 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1109-420G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601681 | |||||||
| chr7:6601752 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(25): Show |
36 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1109-349G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601752 | |||||||
| chr7:6601778 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1109-323G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601778 | |||||||
| chr7:6601820 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0190 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1109-281C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601820 | |||||||
| chr7:6601952 | C | T | 3 | a0001c0002t0001g0187 a0001c0002t0001g0223 a0001c0002t0001g0225 |
3 | HG01978.hp2 NA18949.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1109-149C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6601952 | |||||||
| chr7:6602004 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1109-97C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6602004 | |||||||
| chr7:6602036 | G | T | 7 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0230 others(4): Show |
8 | HG01081.hp2 HG01884.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1109-65G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 4/5 | chr7 | 6602036 | |||||||
| chr7:6602150 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0138 |
2 | NA18942.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1148+10C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602150 | |||||||
| chr7:6602197 | G | C | 2 | a0001c0005t0001g0266 a0001c0005t0001g0267 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1148+57G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602197 | |||||||
| chr7:6602250 | C | G | 21 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(18): Show |
28 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1148+110C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602250 | |||||||
| chr7:6602276 | A | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(18): Show |
28 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1148+136A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602276 | |||||||
| chr7:6602366 | C | T | 4 | a0001c0001t0001g0097 a0002c0004t0001g0014 a0002c0004t0001g0085 others(1): Show |
6 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+226C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602366 | |||||||
| chr7:6602402 | G | T | 1 | a0001c0002t0001g0177 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1148+262G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602402 | |||||||
| chr7:6602412 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(60): Show |
116 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1148+272C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602412 | |||||||
| chr7:6602486 | A | T | 5 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0002c0004t0001g0014 others(2): Show |
7 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+346A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602486 | |||||||
| chr7:6602494 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG02723.hp1 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+354A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602494 | |||||||
| chr7:6602634 | AT | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0031 others(4): Show |
10 | HG01081.hp1 HG02723.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1148+495delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602634 | |||||||
| chr7:6602741 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG02723.hp1 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+601C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602741 | |||||||
| chr7:6602748 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1148+608A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602748 | |||||||
| chr7:6602801 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1148+661C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602801 | |||||||
| chr7:6602828 | G | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1148+688G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602828 | |||||||
| chr7:6602837 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1148+697C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602837 | |||||||
| chr7:6602859 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG02723.hp1 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+719C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602859 | |||||||
| chr7:6602972 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1148+832G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6602972 | |||||||
| chr7:6603079 | G | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0002c0004t0001g0014 others(2): Show |
7 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+939G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603079 | |||||||
| chr7:6603121 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
6 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1148+981G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603121 | |||||||
| chr7:6603146 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
142 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1148+1006C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603146 | |||||||
| chr7:6603193 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1148+1053T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603193 | |||||||
| chr7:6603311 | A | G | 1 | a0001c0002t0001g0168 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1148+1171A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603311 | |||||||
| chr7:6603318 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0087 others(1): Show |
4 | NA18949.hp2 NA18953.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+1178C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603318 | |||||||
| chr7:6603431 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0190 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1148+1291C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603431 | |||||||
| chr7:6603602 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1148+1462G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603602 | |||||||
| chr7:6603707 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1148+1567C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603707 | |||||||
| chr7:6603810 | G | T | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1148+1670G>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603810 | |||||||
| chr7:6603825 | G | C | 1 | a0001c0002t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1148+1685G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603825 | |||||||
| chr7:6603835 | G | A | 1 | a0001c0003t0001g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1148+1695G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603835 | |||||||
| chr7:6603861 | A | G | 4 | a0001c0001t0001g0097 a0002c0004t0001g0014 a0002c0004t0001g0085 others(1): Show |
6 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+1721A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6603861 | |||||||
| chr7:6603998 | TA | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0069 others(2): Show |
7 | HG01169.hp1 HG03130.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+1869delA | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6603998 | ||||||
| chr7:6604033 | A | G | 8 | a0001c0003t0001g0006 a0001c0003t0001g0028 a0001c0003t0001g0029 others(5): Show |
15 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1148+1893A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604033 | |||||||
| chr7:6604064 | T | C | 1 | a0001c0002t0001g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1148+1924T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604064 | |||||||
| chr7:6604069 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.1148+1929A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604069 | |||||||
| chr7:6604128 | T | C | 1 | a0001c0002t0001g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148+1988T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604128 | |||||||
| chr7:6604196 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1148+2056C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604196 | |||||||
| chr7:6604271 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1148+2131A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604271 | |||||||
| chr7:6604390 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1148+2250G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604390 | |||||||
| chr7:6604443 | A | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0100 others(11): Show |
18 | HG00642.hp2 HG01070.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1148+2303A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604443 | |||||||
| chr7:6604619 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0043 |
3 | HG02280.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1148+2479C>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6604619 | |||||||
| chr7:6604910 | G | GA | 3 | a0001c0001t0001g0039 a0001c0001t0001g0228 a0001c0001t0001g0232 |
4 | HG00642.hp2 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+2771dupA | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6604910 | ||||||
| chr7:6605003 | G | GT | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0041 others(2): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1148+2870dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6605003 | ||||||
| chr7:6605078 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(31): Show |
42 | HG00639.hp2 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1149-2882C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605078 | |||||||
| chr7:6605120 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1149-2840G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605120 | |||||||
| chr7:6605213 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-2747T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605213 | |||||||
| chr7:6605329 | A | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0002c0004t0001g0014 others(2): Show |
7 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-2631A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605329 | |||||||
| chr7:6605425 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1149-2535A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605425 | |||||||
| chr7:6605444 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1149-2516A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605444 | |||||||
| chr7:6605481 | A | G | 1 | a0001c0003t0001g0081 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1149-2479A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605481 | |||||||
| chr7:6605541 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1149-2419C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605541 | |||||||
| chr7:6605608 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1149-2352G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605608 | |||||||
| chr7:6605650 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1149-2310C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605650 | |||||||
| chr7:6605688 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1149-2272C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605688 | |||||||
| chr7:6605724 | A | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1149-2236A>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605724 | |||||||
| chr7:6605730 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0237 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-2230G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605730 | |||||||
| chr7:6605754 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02723.hp1 HG03453.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-2206C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6605754 | |||||||
| chr7:6606049 | C | G | 20 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(17): Show |
27 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1149-1911C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606049 | |||||||
| chr7:6606105 | A | G | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1149-1855A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606105 | |||||||
| chr7:6606155 | T | C | 6 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0001c0003t0001g0079 others(3): Show |
8 | HG01109.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-1805T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606155 | |||||||
| chr7:6606264 | C | G | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1149-1696C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606264 | |||||||
| chr7:6606284 | T | G | 1 | a0001c0001t0001g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1149-1676T>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606284 | |||||||
| chr7:6606371 | T | C | 20 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(17): Show |
27 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1149-1589T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606371 | |||||||
| chr7:6606374 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1149-1586G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606374 | |||||||
| chr7:6606385 | CAGAG | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1149-1572_1149-156 others(8): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6606385 | ||||||
| chr7:6606434 | A | G | 3 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0268 |
3 | HG02647.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1149-1526A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606434 | |||||||
| chr7:6606455 | C | T | 5 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0002c0004t0001g0014 others(2): Show |
7 | HG02109.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-1505C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606455 | |||||||
| chr7:6606504 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1149-1456C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606504 | |||||||
| chr7:6606510 | G | A | 2 | a0001c0002t0001g0159 a0001c0002t0001g0160 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1149-1450G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606510 | |||||||
| chr7:6606514 | G | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0118 others(8): Show |
14 | HG00140.hp2 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1149-1446G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606514 | |||||||
| chr7:6606532 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1149-1428G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606532 | |||||||
| chr7:6606567 | G | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-1393G>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606567 | |||||||
| chr7:6606608 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1149-1352C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606608 | |||||||
| chr7:6606647 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1149-1313G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606647 | |||||||
| chr7:6606695 | C | CT | 30 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0074 others(27): Show |
34 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1149-1248dupT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6606695 | ||||||
| chr7:6606695 | CT | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0038 others(11): Show |
19 | HG00735.hp1 HG01175.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1149-1248delT | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6606695 | ||||||
| chr7:6606695 | CTT | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1149-1249_1149-124 others(6): Show |
INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 6606695 | ||||||
| chr7:6606722 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0254 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1149-1238A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606722 | |||||||
| chr7:6606763 | A | G | 1 | a0001c0002t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1149-1197A>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606763 | |||||||
| chr7:6606815 | C | G | 1 | a0001c0002t0001g0171 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1149-1145C>G | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606815 | |||||||
| chr7:6606863 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1149-1097G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606863 | |||||||
| chr7:6606940 | G | A | 1 | a0001c0002t0001g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1149-1020G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6606940 | |||||||
| chr7:6607178 | T | A | 2 | a0001c0002t0001g0121 a0001c0002t0001g0161 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1149-782T>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607178 | |||||||
| chr7:6607227 | T | C | 1 | a0001c0006t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149-733T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607227 | |||||||
| chr7:6607360 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1149-600T>C | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607360 | |||||||
| chr7:6607371 | C | T | 1 | a0001c0002t0001g0175 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1149-589C>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607371 | |||||||
| chr7:6607374 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1149-586G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607374 | |||||||
| chr7:6607448 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1149-512A>T | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607448 | |||||||
| chr7:6607753 | G | A | 1 | a0001c0006t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149-207G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607753 | |||||||
| chr7:6607912 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1149-48G>A | INTS15 | ENSG00000146576.13 | transcript | ENST00000344417.10 | protein_coding | 5/5 | chr7 | 6607912 |