Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54973 |
| ensemblid | ENSG00000127054.22 |
| hgncid | 26052 |
| symbol | INTS11 |
| name | integrator complex subunit 11 |
| refseq_nuc | NM_017871.6 |
| refseq_prot | NP_060341.2 |
| ensembl_nuc | ENST00000435064.6 |
| ensembl_prot | ENSP00000413493.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 1311600 |
| end | 1324660 |
| strand | - |
| ver | v1.2 |
| region | chr1:1311600-1324660 |
| region5000 | chr1:1306600-1329660 |
| regionname0 | INTS11_chr1_1311600_1324660 |
| regionname5000 | INTS11_chr1_1306600_1329660 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 600 | 352 | 91 | 59 | 136 | 16 | 48 | 96 | INTS11_chr1_1306600_1329660 | INTS11 | MPEIR others(595): Show |
chr1 | 1306600 | 1329660 |
| a0002 | 0/0 | 16 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | MPEIR others(11): Show |
chr1 | 1306600 | 1329660 |
| a0003 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | MPEIR others(595): Show |
chr1 | 1306600 | 1329660 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1800 | 177 | 27 | 25 | 94 | 6 | 25 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0002 | 1/0 | 1800 | 96 | 46 | 6 | 37 | 0 | 6 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0003 | 0/1 | 1800 | 56 | 6 | 25 | 1 | 8 | 15 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0004 | 0/0 | 1800 | 6 | 5 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0005 | 0/0 | 1800 | 6 | 0 | 2 | 0 | 2 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0006 | 0/0 | 1800 | 3 | 0 | 0 | 3 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0007 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0008 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0009 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0010 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0012 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0001c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0002c0014 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 | ||
| a0003c0011 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | ATGCC others(1795): Show |
chr1 | 1306600 | 1329660 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2114 | 174 | 26 | 24 | 93 | 6 | 25 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0001t0003 | 0/0 | 2114 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0001t0006 | 0/0 | 2114 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0001t0008 | 0/0 | 2114 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0002t0001 | 1/0 | 2114 | 85 | 37 | 4 | 37 | 0 | 6 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0002t0002 | 0/0 | 2113 | 10 | 8 | 2 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2108): Show |
chr1 | 1306600 | 1329660 |
| a0001c0002t0005 | 0/0 | 2114 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0003t0001 | 0/1 | 2114 | 55 | 6 | 24 | 1 | 8 | 15 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0003t0004 | 0/0 | 2114 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0004t0001 | 0/0 | 2114 | 6 | 5 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0005t0001 | 0/0 | 2114 | 6 | 0 | 2 | 0 | 2 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0006t0001 | 0/0 | 2114 | 3 | 0 | 0 | 3 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0007t0001 | 0/0 | 2114 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0008t0001 | 0/0 | 2114 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0009t0001 | 0/0 | 2114 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0010t0007 | 0/0 | 2113 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2108): Show |
chr1 | 1306600 | 1329660 |
| a0001c0012t0001 | 0/0 | 2114 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0001c0013t0001 | 0/0 | 2114 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0002c0014t0001 | 0/0 | 2114 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| a0003c0011t0001 | 0/0 | 2114 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | GCAGT others(2109): Show |
chr1 | 1306600 | 1329660 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 0 | 3 | 16 | 1 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 2 | 10 | 1 | 3 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0003 | 0/0 | 15 | 1 | 3 | 7 | 1 | 3 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0004 | 1/0 | 10 | 2 | 0 | 6 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0013 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0014 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0002t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0005 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0003t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0004t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0006t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0007t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0008t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0009t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0010t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0012t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0001c0013t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0002c0014t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| a0003c0011t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0012 | EUR | GBR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0135 | EUR | FIN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | FIN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00733 | hp1 | a0001 | c0003 | t0004 | g0129 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00738 | hp1 | a0002 | c0014 | t0001 | g0132 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0191 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0192 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0034 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0190 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0137 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01517 | hp2 | a0001 | c0005 | t0001 | g0173 | EUR | IBS | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0036 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0204 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02027 | hp1 | a0001 | c0009 | t0001 | g0066 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CDX | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CDX | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0133 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0116 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02723 | hp1 | a0001 | c0013 | t0001 | g0183 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0185 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0186 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0039 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0184 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0172 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03453 | hp1 | a0003 | c0011 | t0001 | g0059 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0035 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0035 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0130 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0124 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0012 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0037 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0193 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0119 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0127 | SAS | STU | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18906 | hp1 | a0001 | c0007 | t0001 | g0174 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0030 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18947 | hp1 | a0001 | c0006 | t0001 | g0030 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18982 | hp2 | a0001 | c0006 | t0001 | g0099 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19030 | hp2 | a0001 | c0010 | t0007 | g0202 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19043 | hp1 | a0001 | c0008 | t0001 | g0043 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | ASW | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | ASW | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0034 | EUR | TSI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0122 | EUR | TSI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0138 | EUR | TSI | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | GIH | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0201 | SAS | GIH | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0187 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02109 | hp1 | a0001 | c0012 | t0001 | g0188 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02559 | hp1 | a0001 | c0007 | t0001 | g0179 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | USA | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20300 | hp1 | a0001 | c0008 | t0001 | g0043 | AFR | USA | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | LWK | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0117 | REF | REF | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0004 | REF | REF | INTS11_chr1_1306600_1329660 | INTS11 | chr1 | 1306600 | 1329660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1313038 | C | G | 1 | a0003 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1128G>C | p.Gln376His | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 11/17 | 1180/2114 | 1128/1803 | 376/600 | chr1 | 1313038 | |||
| chr1:1321073 | G | A | 1 | a0002 | 1 | HG00738.hp1 | stop_gained | HIGH | c.49C>T | p.Arg17* | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/17 | 101/2114 | 49/1803 | 17/600 | chr1 | 1321073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1311922 | G | A | 1 | a0001c0009 | 1 | HG02027.hp1 | splice_region_variant&synonymous_variant | LOW | c.1740C>T | p.Asp580Asp | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 1792/2114 | 1740/1803 | 580/600 | chr1 | 1311922 | |||
| chr1:1312114 | T | C | 3 | a0001c0003 a0001c0007 a0002c0014 |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
synonymous_variant | LOW | c.1641A>G | p.Pro547Pro | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 16/17 | 1693/2114 | 1641/1803 | 547/600 | chr1 | 1312114 | |||
| chr1:1312800 | G | A | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1281C>T | p.Ile427Ile | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 12/17 | 1333/2114 | 1281/1803 | 427/600 | chr1 | 1312800 | |||
| chr1:1313807 | G | A | 3 | a0001c0003 a0001c0012 a0002c0014 |
57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
synonymous_variant | LOW | c.882C>T | p.Phe294Phe | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 9/17 | 934/2114 | 882/1803 | 294/600 | chr1 | 1313807 | |||
| chr1:1314890 | G | A | 1 | a0001c0008 | 2 | NA19043.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.636C>T | p.Asp212Asp | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/17 | 688/2114 | 636/1803 | 212/600 | chr1 | 1314890 | |||
| chr1:1314938 | G | A | 3 | a0001c0004 a0001c0012 a0003c0011 |
8 | HG01123.hp1 HG02109.hp1 HG02922.hp1 others(5): Show |
synonymous_variant | LOW | c.588C>T | p.Arg196Arg | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/17 | 640/2114 | 588/1803 | 196/600 | chr1 | 1314938 | |||
| chr1:1315577 | G | A | 1 | a0001c0005 | 6 | HG01192.hp1 HG01261.hp1 HG01516.hp2 others(3): Show |
synonymous_variant | LOW | c.471C>T | p.His157His | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 5/17 | 523/2114 | 471/1803 | 157/600 | chr1 | 1315577 | |||
| chr1:1319461 | C | G | 5 | a0001c0001 a0001c0003 a0001c0006 others(2): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
synonymous_variant | LOW | c.264G>C | p.Gly88Gly | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/17 | 316/2114 | 264/1803 | 88/600 | chr1 | 1319461 | |||
| chr1:1320485 | T | C | 1 | a0001c0006 | 3 | NA18940.hp1 NA18947.hp1 NA18982.hp2 |
synonymous_variant | LOW | c.171A>G | p.Leu57Leu | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/17 | 223/2114 | 171/1803 | 57/600 | chr1 | 1320485 | |||
| chr1:1321061 | G | A | 1 | a0001c0013 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.61C>T | p.Leu21Leu | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/17 | 113/2114 | 61/1803 | 21/600 | chr1 | 1321061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1311706 | G | A | 1 | a0001c0002t0005 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 153 | chr1 | 1311706 | ||||||
| chr1:1311713 | G | A | 2 | a0001c0002t0002 a0001c0002t0005 |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 146 | chr1 | 1311713 | ||||||
| chr1:1311747 | G | A | 1 | a0001c0001t0006 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 112 | chr1 | 1311747 | ||||||
| chr1:1311805 | AG | A | 2 | a0001c0002t0002 a0001c0010t0007 |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*53delC | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 53 | chr1 | 1311805 | ||||||
| chr1:1311814 | C | G | 1 | a0001c0003t0004 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 45 | chr1 | 1311814 | ||||||
| chr1:1311824 | G | A | 1 | a0001c0001t0008 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 17/17 | 35 | chr1 | 1311824 | ||||||
| chr1:1324626 | C | G | 1 | a0001c0001t0003 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/17 | 18 | chr1 | 1324626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1311971 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1737+47T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 16/16 | chr1 | 1311971 | |||||||
| chr1:1311991 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1737+27G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 16/16 | chr1 | 1311991 | |||||||
| chr1:1312162 | G | A | 4 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0161 others(1): Show |
6 | HG02027.hp2 NA18959.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608-15C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312162 | |||||||
| chr1:1312175 | C | T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(6): Show |
22 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1608-28G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312175 | |||||||
| chr1:1312198 | T | TG | 24 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0068 others(21): Show |
30 | HG00280.hp2 HG00639.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1607+27dupC | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | T | TGG | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(35): Show |
68 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.1607+26_1607+27dup others(2): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | T | TGGG | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(44): Show |
96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1607+25_1607+27dup others(3): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | T | TGGGGGG | 17 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0036 others(14): Show |
29 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1607+22_1607+27dup others(6): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | T | TGGGGGGG | 14 | a0001c0003t0001g0012 a0001c0003t0001g0034 a0001c0003t0001g0035 others(11): Show |
20 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1607+21_1607+27dup others(7): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | T | TGGGGGGG others(5): Show |
1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1607+27_1607+28ins others(12): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312198 | TG | T | 18 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0021 others(15): Show |
27 | HG00544.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1607+27delC | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312198 | |||||||
| chr1:1312208 | G | T | 2 | a0001c0005t0001g0190 a0001c0005t0001g0201 |
2 | HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1607+18C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312208 | |||||||
| chr1:1312220 | G | C | 1 | a0001c0003t0001g0137 | 1 | HG01517.hp1 | splice_region_variant&intron_variant | LOW | c.1607+6C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 15/16 | chr1 | 1312220 | |||||||
| chr1:1312384 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1465-16T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 14/16 | chr1 | 1312384 | |||||||
| chr1:1312400 | C | T | 1 | a0001c0003t0001g0139 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1465-32G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 14/16 | chr1 | 1312400 | |||||||
| chr1:1312425 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1464+15G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 14/16 | chr1 | 1312425 | |||||||
| chr1:1312563 | A | ACCCTGCC others(3): Show |
2 | a0001c0003t0001g0133 a0001c0003t0001g0136 |
2 | HG02486.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1402+20_1402+29dup others(10): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 13/16 | chr1 | 1312563 | |||||||
| chr1:1312715 | AAG | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0108 |
3 | NA18954.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1295-17_1295-16del others(2): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 12/16 | chr1 | 1312715 | |||||||
| chr1:1312752 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1294+35C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 12/16 | chr1 | 1312752 | |||||||
| chr1:1312958 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1132-9C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 11/16 | chr1 | 1312958 | |||||||
| chr1:1312973 | C | T | 2 | a0001c0003t0001g0123 a0001c0003t0001g0130 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1132-24G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 11/16 | chr1 | 1312973 | |||||||
| chr1:1313181 | C | T | 1 | a0001c0003t0001g0204 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1042-57G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313181 | |||||||
| chr1:1313206 | C | A | 5 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0186 others(2): Show |
6 | HG01123.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-82G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313206 | |||||||
| chr1:1313219 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042-95A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313219 | |||||||
| chr1:1313240 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1042-116G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313240 | |||||||
| chr1:1313241 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1042-117C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313241 | |||||||
| chr1:1313253 | C | A | 1 | a0001c0002t0001g0160 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1042-129G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313253 | |||||||
| chr1:1313288 | ACTGTCCA others(11): Show |
A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1042-182_1042-165d others(20): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313288 | |||||||
| chr1:1313327 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1041+182C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313327 | |||||||
| chr1:1313341 | C | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1041+168G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313341 | |||||||
| chr1:1313414 | G | A | 4 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0186 others(1): Show |
5 | HG02109.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+95C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313414 | |||||||
| chr1:1313414 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1041+95C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 10/16 | chr1 | 1313414 | |||||||
| chr1:1313640 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.958-48G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 9/16 | chr1 | 1313640 | |||||||
| chr1:1313707 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.957+25A>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 9/16 | chr1 | 1313707 | |||||||
| chr1:1313714 | C | T | 1 | a0001c0003t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.957+18G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 9/16 | chr1 | 1313714 | |||||||
| chr1:1313974 | G | C | 1 | a0001c0002t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.768-53C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 8/16 | chr1 | 1313974 | |||||||
| chr1:1314028 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.768-107C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 8/16 | chr1 | 1314028 | |||||||
| chr1:1314439 | G | A | 4 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0161 others(1): Show |
6 | HG02027.hp2 NA18959.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-74C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314439 | |||||||
| chr1:1314517 | A | G | 1 | a0001c0002t0001g0044 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703-152T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314517 | |||||||
| chr1:1314586 | G | A | 1 | a0001c0003t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.703-221C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314586 | |||||||
| chr1:1314608 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00558.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.702+216G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314608 | |||||||
| chr1:1314625 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+199C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314625 | |||||||
| chr1:1314644 | C | T | 1 | a0001c0013t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.702+180G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314644 | |||||||
| chr1:1314808 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.702+16G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 7/16 | chr1 | 1314808 | |||||||
| chr1:1315017 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.564-55C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315017 | |||||||
| chr1:1315050 | G | A | 1 | a0001c0002t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.564-88C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315050 | |||||||
| chr1:1315162 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.564-200C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315162 | |||||||
| chr1:1315249 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0090 |
2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.563+155G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315249 | |||||||
| chr1:1315286 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.563+118C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315286 | |||||||
| chr1:1315369 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.563+35C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 6/16 | chr1 | 1315369 | |||||||
| chr1:1315447 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.529-9G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 5/16 | chr1 | 1315447 | |||||||
| chr1:1315624 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.430-6C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315624 | |||||||
| chr1:1315706 | C | CGGGGGTG others(8): Show |
1 | a0001c0003t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.430-103_430-89dupA others(14): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315706 | |||||||
| chr1:1315712 | TGGGGA | T | 11 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(8): Show |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-99_430-95delTC others(3): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315712 | |||||||
| chr1:1315728 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-110T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315728 | |||||||
| chr1:1315747 | GGCGGGAG others(33): Show |
G | 1 | a0001c0003t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430-169_430-130del others(40): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315747 | |||||||
| chr1:1315752 | GAGCGAGG others(35): Show |
G | 9 | a0001c0003t0001g0010 a0001c0003t0001g0034 a0001c0003t0001g0035 others(6): Show |
11 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-176_430-135del others(42): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315752 | |||||||
| chr1:1315778 | G | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-160C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315778 | |||||||
| chr1:1315779 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-161T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315779 | |||||||
| chr1:1315797 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.430-179G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315797 | |||||||
| chr1:1315798 | G | A | 2 | a0001c0002t0001g0158 a0001c0002t0001g0162 |
2 | NA18943.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.430-180C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315798 | |||||||
| chr1:1315807 | AGGGGCAG others(15): Show |
A | 13 | a0001c0001t0001g0094 a0001c0002t0002g0051 a0001c0002t0002g0052 others(10): Show |
13 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-211_430-190del others(22): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315807 | |||||||
| chr1:1315822 | G | GGGGGGC | 5 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0112 others(2): Show |
6 | HG01891.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-210_430-205dup others(6): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315822 | |||||||
| chr1:1315828 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.430-210G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315828 | |||||||
| chr1:1315829 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.430-211C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315829 | |||||||
| chr1:1315847 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.430-229C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315847 | |||||||
| chr1:1315852 | G | A | 16 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0171 others(13): Show |
19 | HG01346.hp1 HG01891.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.430-234C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315852 | |||||||
| chr1:1315891 | T | G | 5 | a0001c0002t0001g0042 a0001c0002t0001g0156 a0001c0002t0001g0159 others(2): Show |
6 | HG00558.hp1 HG02071.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-273A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315891 | |||||||
| chr1:1315929 | C | T | 1 | a0001c0003t0001g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.430-311G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315929 | |||||||
| chr1:1315942 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0090 |
2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.430-324G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315942 | |||||||
| chr1:1315943 | G | A | 7 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0185 others(4): Show |
8 | HG01123.hp1 HG02109.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-325C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315943 | |||||||
| chr1:1315953 | G | A | 1 | a0001c0002t0001g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.430-335C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315953 | |||||||
| chr1:1315996 | G | T | 1 | a0001c0002t0001g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.430-378C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1315996 | |||||||
| chr1:1316008 | A | G | 7 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0185 others(4): Show |
8 | HG01123.hp1 HG02109.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-390T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316008 | |||||||
| chr1:1316042 | G | A | 7 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0185 others(4): Show |
8 | HG01123.hp1 HG02109.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-424C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316042 | |||||||
| chr1:1316154 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-536A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316154 | |||||||
| chr1:1316407 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.430-789C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316407 | |||||||
| chr1:1316467 | T | C | 1 | a0001c0002t0005g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430-849A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316467 | |||||||
| chr1:1316564 | C | A | 1 | a0001c0002t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430-946G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316564 | |||||||
| chr1:1316575 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.430-957T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316575 | |||||||
| chr1:1316608 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.430-990C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316608 | |||||||
| chr1:1316613 | C | G | 1 | a0001c0002t0001g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430-995G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316613 | |||||||
| chr1:1316616 | T | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-998A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316616 | |||||||
| chr1:1316628 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.430-1010A>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316628 | |||||||
| chr1:1316646 | C | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-1028G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316646 | |||||||
| chr1:1316650 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-1032A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316650 | |||||||
| chr1:1316660 | C | T | 2 | a0001c0001t0001g0089 a0001c0002t0001g0175 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.430-1042G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316660 | |||||||
| chr1:1316662 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.430-1044A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316662 | |||||||
| chr1:1316742 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | NA18947.hp2 NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.430-1124G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316742 | |||||||
| chr1:1316754 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.430-1136C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316754 | |||||||
| chr1:1316834 | GAACTGCT others(292): Show |
G | 2 | a0001c0003t0001g0124 a0001c0003t0001g0125 |
2 | HG01081.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.430-1515_430-1217d others(2): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316834 | |||||||
| chr1:1316881 | G | A | 3 | a0001c0002t0002g0056 a0001c0002t0002g0057 a0001c0002t0002g0058 |
3 | HG00642.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430-1263C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316881 | |||||||
| chr1:1316929 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.430-1311T>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1316929 | |||||||
| chr1:1317020 | C | T | 2 | a0001c0003t0001g0016 a0002c0014t0001g0132 |
3 | HG00738.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.430-1402G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317020 | |||||||
| chr1:1317041 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.430-1423C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317041 | |||||||
| chr1:1317084 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-1466T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317084 | |||||||
| chr1:1317116 | G | A | 11 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(8): Show |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-1498C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317116 | |||||||
| chr1:1317134 | A | C | 2 | a0001c0003t0001g0124 a0001c0003t0001g0125 |
2 | HG01081.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.430-1516T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317134 | |||||||
| chr1:1317135 | A | C | 2 | a0001c0003t0001g0124 a0001c0003t0001g0125 |
2 | HG01081.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.430-1517T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317135 | |||||||
| chr1:1317160 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01069.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.430-1542G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317160 | |||||||
| chr1:1317180 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-1562T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317180 | |||||||
| chr1:1317239 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0084 |
2 | HG00597.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.430-1621T>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317239 | |||||||
| chr1:1317278 | C | T | 7 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(4): Show |
7 | HG01099.hp1 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-1660G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317278 | |||||||
| chr1:1317350 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.430-1732C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317350 | |||||||
| chr1:1317370 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.430-1752C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317370 | |||||||
| chr1:1317391 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430-1773T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317391 | |||||||
| chr1:1317485 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG00323.hp2 HG00597.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.429+1811G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317485 | |||||||
| chr1:1317565 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.429+1731A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317565 | |||||||
| chr1:1317566 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.429+1730G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317566 | |||||||
| chr1:1317644 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.429+1652G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317644 | |||||||
| chr1:1317772 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.429+1524T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317772 | |||||||
| chr1:1317789 | TAAAATCT others(15): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.429+1485_429+1506d others(24): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317789 | |||||||
| chr1:1317809 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1487C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317809 | |||||||
| chr1:1317934 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1362A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317934 | |||||||
| chr1:1317982 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1314A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1317982 | |||||||
| chr1:1318006 | T | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1290A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318006 | |||||||
| chr1:1318047 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1249A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318047 | |||||||
| chr1:1318220 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.429+1076A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318220 | |||||||
| chr1:1318462 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.429+834T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318462 | |||||||
| chr1:1318501 | C | G | 1 | a0001c0002t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.429+795G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318501 | |||||||
| chr1:1318519 | C | T | 11 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(8): Show |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+777G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318519 | |||||||
| chr1:1318641 | C | G | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+655G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318641 | |||||||
| chr1:1318650 | A | C | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+646T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318650 | |||||||
| chr1:1318669 | T | C | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+627A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318669 | |||||||
| chr1:1318677 | C | A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+619G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318677 | |||||||
| chr1:1318689 | A | C | 10 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(7): Show |
23 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.429+607T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318689 | |||||||
| chr1:1318722 | T | C | 2 | a0001c0005t0001g0173 a0001c0005t0001g0190 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.429+574A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318722 | |||||||
| chr1:1318731 | C | T | 1 | a0001c0003t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.429+565G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318731 | |||||||
| chr1:1318756 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.429+540C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318756 | |||||||
| chr1:1318769 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.429+527A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318769 | |||||||
| chr1:1318791 | G | C | 13 | a0001c0001t0001g0096 a0001c0002t0002g0051 a0001c0002t0002g0052 others(10): Show |
13 | HG00642.hp2 HG01099.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+505C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318791 | |||||||
| chr1:1318849 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+447C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318849 | |||||||
| chr1:1318875 | G | A | 16 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0171 others(13): Show |
19 | HG01346.hp1 HG01891.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+421C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318875 | |||||||
| chr1:1318951 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.429+345G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1318951 | |||||||
| chr1:1319056 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.429+240T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1319056 | |||||||
| chr1:1319063 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.429+233C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1319063 | |||||||
| chr1:1319123 | C | G | 1 | a0001c0001t0001g0011 | 4 | HG03239.hp1 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+173G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1319123 | |||||||
| chr1:1319219 | T | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+77A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 4/16 | chr1 | 1319219 | |||||||
| chr1:1319648 | G | A | 2 | a0001c0003t0001g0039 a0001c0003t0001g0138 |
3 | HG00741.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.201-124C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319648 | |||||||
| chr1:1319712 | A | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201-188T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319712 | |||||||
| chr1:1319750 | G | A | 17 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(14): Show |
31 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.201-226C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319750 | |||||||
| chr1:1319796 | A | G | 1 | a0001c0008t0001g0043 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.201-272T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319796 | |||||||
| chr1:1319804 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.201-280C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319804 | |||||||
| chr1:1319819 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.201-295C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319819 | |||||||
| chr1:1319871 | G | C | 6 | a0001c0005t0001g0173 a0001c0005t0001g0190 a0001c0005t0001g0191 others(3): Show |
6 | HG01192.hp1 HG01261.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-347C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319871 | |||||||
| chr1:1319883 | C | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201-359G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319883 | |||||||
| chr1:1319907 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.201-383G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319907 | |||||||
| chr1:1319966 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
4 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-442T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1319966 | |||||||
| chr1:1320023 | TG | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.200+432delC | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320023 | |||||||
| chr1:1320057 | G | A | 11 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(8): Show |
11 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.200+399C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320057 | |||||||
| chr1:1320145 | C | A | 1 | a0001c0003t0001g0139 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.200+311G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320145 | |||||||
| chr1:1320252 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.200+204C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320252 | |||||||
| chr1:1320378 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.200+78C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320378 | |||||||
| chr1:1320384 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.200+72C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 3/16 | chr1 | 1320384 | |||||||
| chr1:1320598 | C | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-69G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320598 | |||||||
| chr1:1320653 | C | T | 17 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(14): Show |
31 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.127-124G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320653 | |||||||
| chr1:1320751 | G | A | 1 | a0001c0002t0001g0048 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-222C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320751 | |||||||
| chr1:1320795 | G | A | 2 | a0001c0002t0001g0044 a0001c0002t0001g0182 |
3 | HG03453.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126+201C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320795 | |||||||
| chr1:1320870 | C | A | 9 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(6): Show |
22 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+126G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320870 | |||||||
| chr1:1320935 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+61T>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320935 | |||||||
| chr1:1320944 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+52G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 2/16 | chr1 | 1320944 | |||||||
| chr1:1321127 | G | GC | 7 | a0001c0001t0001g0083 a0001c0001t0001g0115 a0001c0001t0001g0207 others(4): Show |
7 | HG01192.hp1 HG02074.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-35dupG | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321127 | |||||||
| chr1:1321150 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0086 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.29-57G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321150 | |||||||
| chr1:1321187 | C | T | 1 | a0001c0004t0001g0186 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.29-94G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321187 | |||||||
| chr1:1321228 | G | A | 3 | a0001c0003t0001g0035 a0001c0003t0001g0122 a0001c0003t0001g0128 |
4 | HG03491.hp1 HG03492.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-135C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321228 | |||||||
| chr1:1321264 | G | GGGACCAT others(9): Show |
1 | a0001c0001t0001g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.29-187_29-172dupGT others(14): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321264 | |||||||
| chr1:1321503 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.29-410G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321503 | |||||||
| chr1:1321555 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.29-462C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321555 | |||||||
| chr1:1321577 | G | T | 8 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(5): Show |
8 | HG01099.hp1 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-484C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321577 | |||||||
| chr1:1321667 | C | G | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-574G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321667 | |||||||
| chr1:1321825 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.29-732C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321825 | |||||||
| chr1:1321991 | C | G | 3 | a0001c0005t0001g0191 a0001c0005t0001g0192 a0001c0005t0001g0193 |
3 | HG01192.hp1 HG01261.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.29-898G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1321991 | |||||||
| chr1:1322113 | T | G | 1 | a0001c0003t0004g0129 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.29-1020A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322113 | |||||||
| chr1:1322201 | C | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-1108G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322201 | |||||||
| chr1:1322213 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.29-1120T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322213 | |||||||
| chr1:1322254 | T | C | 1 | a0001c0002t0005g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29-1161A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322254 | |||||||
| chr1:1322339 | A | C | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-1246T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322339 | |||||||
| chr1:1322427 | C | A | 7 | a0001c0004t0001g0045 a0001c0004t0001g0172 a0001c0004t0001g0185 others(4): Show |
8 | HG01123.hp1 HG02109.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1334G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322427 | |||||||
| chr1:1322469 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.29-1376C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322469 | |||||||
| chr1:1322517 | G | C | 2 | a0001c0003t0001g0123 a0001c0003t0001g0130 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.29-1424C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322517 | |||||||
| chr1:1322548 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.29-1455C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322548 | |||||||
| chr1:1322549 | G | A | 2 | a0001c0005t0001g0173 a0001c0005t0001g0190 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.29-1456C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322549 | |||||||
| chr1:1322563 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-1470C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322563 | |||||||
| chr1:1322655 | G | C | 2 | a0001c0001t0001g0084 a0001c0002t0001g0046 |
3 | HG00597.hp1 HG02165.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.29-1562C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322655 | |||||||
| chr1:1322709 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.29-1616C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322709 | |||||||
| chr1:1322712 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.29-1619C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322712 | |||||||
| chr1:1322746 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.29-1653G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322746 | |||||||
| chr1:1322752 | C | CG | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0022 others(63): Show |
96 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.29-1660dupC | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322752 | |||||||
| chr1:1322866 | A | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.28+1715T>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322866 | |||||||
| chr1:1322879 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG03239.hp1 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+1702C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322879 | |||||||
| chr1:1322952 | TGAAAGAT others(2): Show |
T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
5 | NA18954.hp2 NA18983.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+1620_28+1628del others(9): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1322952 | |||||||
| chr1:1323122 | G | GGTGTTCA others(5): Show |
1 | a0001c0002t0001g0166 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.28+1447_28+1458dup others(12): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323122 | |||||||
| chr1:1323147 | C | T | 1 | a0001c0003t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.28+1434G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323147 | |||||||
| chr1:1323341 | C | T | 4 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(1): Show |
4 | HG02258.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+1240G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323341 | |||||||
| chr1:1323353 | G | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01243.hp2 HG03486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+1228C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323353 | |||||||
| chr1:1323364 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.28+1217A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323364 | |||||||
| chr1:1323438 | G | A | 3 | a0001c0005t0001g0191 a0001c0005t0001g0192 a0001c0005t0001g0193 |
3 | HG01192.hp1 HG01261.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.28+1143C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323438 | |||||||
| chr1:1323576 | A | T | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28+1005T>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323576 | |||||||
| chr1:1323579 | A | AT | 9 | a0001c0001t0001g0073 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
9 | HG01975.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.28+1001dupA | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323579 | |||||||
| chr1:1323631 | G | A | 1 | a0001c0002t0001g0194 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.28+950C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323631 | |||||||
| chr1:1323787 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.28+794C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323787 | |||||||
| chr1:1323853 | G | GA | 9 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0021 others(6): Show |
22 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.28+727dupT | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323853 | |||||||
| chr1:1323919 | ACTGGGGG others(9): Show |
A | 2 | a0001c0002t0002g0051 a0001c0002t0002g0053 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28+646_28+661delCC others(14): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323919 | |||||||
| chr1:1323943 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+638C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323943 | |||||||
| chr1:1323953 | T | C | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.28+628A>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323953 | |||||||
| chr1:1323955 | G | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+626C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323955 | |||||||
| chr1:1323956 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+625C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323956 | |||||||
| chr1:1323959 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+622A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323959 | |||||||
| chr1:1323963 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+618G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323963 | |||||||
| chr1:1323964 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+617A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323964 | |||||||
| chr1:1323967 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+614C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323967 | |||||||
| chr1:1323968 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28+613G>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323968 | |||||||
| chr1:1323971 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+610T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323971 | |||||||
| chr1:1323975 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+606C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323975 | |||||||
| chr1:1323980 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+601C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323980 | |||||||
| chr1:1323982 | G | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+599C>G | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323982 | |||||||
| chr1:1323983 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+598T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323983 | |||||||
| chr1:1323987 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+594T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323987 | |||||||
| chr1:1323990 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.28+591C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323990 | |||||||
| chr1:1323999 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+582T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1323999 | |||||||
| chr1:1324007 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+574A>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324007 | |||||||
| chr1:1324007 | T | G | 1 | a0001c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.28+574A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324007 | |||||||
| chr1:1324011 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+570G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324011 | |||||||
| chr1:1324011 | C | G | 1 | a0001c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.28+570G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324011 | |||||||
| chr1:1324012 | T | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(5): Show |
15 | HG02630.hp2 NA18941.hp2 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.28+569A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324012 | |||||||
| chr1:1324015 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
6 | HG02630.hp2 NA18954.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+566C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324015 | |||||||
| chr1:1324023 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+558A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324023 | |||||||
| chr1:1324029 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+552C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324029 | |||||||
| chr1:1324031 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+550T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324031 | |||||||
| chr1:1324034 | G | GA | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+546_28+547insT | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324034 | |||||||
| chr1:1324037 | GC | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+543delG | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324037 | |||||||
| chr1:1324046 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+535C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324046 | |||||||
| chr1:1324055 | GCTGAGGG others(1): Show |
G | 2 | a0001c0003t0001g0016 a0002c0014t0001g0132 |
4 | HG00738.hp1 HG01361.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+518_28+525delTC others(6): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324055 | |||||||
| chr1:1324059 | A | AGGGTCTG others(1): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+521_28+522insGC others(6): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324059 | |||||||
| chr1:1324063 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+518T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324063 | |||||||
| chr1:1324067 | A | AGGGGCTG others(89): Show |
1 | a0001c0002t0001g0156 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.28+513_28+514insCC others(94): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324067 | |||||||
| chr1:1324067 | A | AGGGGCTG others(73): Show |
7 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(4): Show |
7 | HG01099.hp1 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+513_28+514insCC others(78): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324067 | |||||||
| chr1:1324075 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+506T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324075 | |||||||
| chr1:1324094 | G | GGCTGGGG others(65): Show |
1 | a0001c0002t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.28+486_28+487insTC others(70): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324094 | |||||||
| chr1:1324110 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+471C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324110 | |||||||
| chr1:1324115 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+466T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324115 | |||||||
| chr1:1324119 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+462A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324119 | |||||||
| chr1:1324123 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+458G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324123 | |||||||
| chr1:1324133 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.28+448C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324133 | |||||||
| chr1:1324134 | G | GGCTGGGG others(49): Show |
1 | a0001c0008t0001g0043 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.28+446_28+447insTC others(54): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324134 | |||||||
| chr1:1324134 | G | GGCTGGGG others(33): Show |
50 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0020 others(47): Show |
68 | HG00642.hp2 HG01099.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.28+446_28+447insTC others(38): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324134 | |||||||
| chr1:1324134 | G | GGCTGGGG others(161): Show |
1 | a0001c0005t0001g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.28+446_28+447insTC others(166): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324134 | |||||||
| chr1:1324139 | GGGGGCTG others(25): Show |
G | 9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01975.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.28+410_28+441delTC others(30): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324139 | |||||||
| chr1:1324144 | C | CTGGGAGG others(34): Show |
1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28+436_28+437insAG others(39): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324144 | |||||||
| chr1:1324148 | G | GGGGCTGC others(1): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+432_28+433insAG others(6): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324148 | |||||||
| chr1:1324149 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.28+432C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324149 | |||||||
| chr1:1324155 | A | AGAGGCTG others(17): Show |
19 | a0001c0001t0001g0038 a0001c0001t0001g0061 a0001c0003t0001g0005 others(16): Show |
36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.28+425_28+426insCC others(22): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324155 | |||||||
| chr1:1324157 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
195 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.28+424C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324157 | |||||||
| chr1:1324163 | G | GGGAGCTG others(25): Show |
1 | a0001c0002t0001g0040 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.28+417_28+418insTC others(30): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324163 | |||||||
| chr1:1324165 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+416C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324165 | |||||||
| chr1:1324166 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
181 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.28+415C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324166 | |||||||
| chr1:1324167 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+414C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324167 | |||||||
| chr1:1324171 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
195 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.28+410T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324171 | |||||||
| chr1:1324172 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0142 others(4): Show |
14 | NA18941.hp2 NA18948.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+409C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(65): Show |
17 | a0001c0003t0001g0010 a0001c0003t0001g0034 a0001c0003t0001g0035 others(14): Show |
23 | HG00639.hp1 HG00733.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.28+408_28+409insTC others(70): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(81): Show |
1 | a0003c0011t0001g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28+408_28+409insTC others(86): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(57): Show |
1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.28+408_28+409insTC others(62): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(65): Show |
62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.28+408_28+409insTC others(70): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(73): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | NA18947.hp2 NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.28+408_28+409insTC others(78): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(66): Show |
1 | a0001c0001t0001g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.28+408_28+409insTC others(71): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(73): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
16 | HG00280.hp2 HG01123.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+408_28+409insTC others(78): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGAGCTGG others(74): Show |
1 | a0001c0001t0001g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.28+408_28+409insTC others(79): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGGGCTCG others(41): Show |
17 | a0001c0001t0001g0038 a0001c0003t0001g0005 a0001c0003t0001g0012 others(14): Show |
34 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.28+408_28+409insTC others(46): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324172 | G | GGGGCTCG others(42): Show |
1 | a0001c0003t0001g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.28+408_28+409insTC others(47): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324172 | |||||||
| chr1:1324174 | G | A | 1 | a0001c0010t0007g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28+407C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324174 | |||||||
| chr1:1324179 | G | GGGGGCTG others(57): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
5 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+401_28+402insAC others(62): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324179 | |||||||
| chr1:1324179 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.28+402C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324179 | |||||||
| chr1:1324181 | A | AGACTGGA others(9): Show |
1 | a0001c0001t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.28+399_28+400insCC others(14): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324181 | |||||||
| chr1:1324181 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.28+400T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324181 | |||||||
| chr1:1324189 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.28+392T>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324189 | |||||||
| chr1:1324220 | G | GGGGCTGA others(161): Show |
1 | a0001c0002t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28+360_28+361insAG others(166): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324220 | |||||||
| chr1:1324220 | G | GGGGCTGA others(161): Show |
7 | a0001c0002t0002g0051 a0001c0002t0002g0052 a0001c0002t0002g0053 others(4): Show |
7 | HG00642.hp2 HG01099.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+360_28+361insAG others(166): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324220 | |||||||
| chr1:1324220 | G | GGGGCTGA others(153): Show |
1 | a0001c0002t0002g0060 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.28+360_28+361insAG others(158): Show |
INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324220 | |||||||
| chr1:1324220 | G | T | 2 | a0001c0002t0002g0058 a0003c0011t0001g0059 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.28+361C>A | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324220 | |||||||
| chr1:1324241 | T | A | 1 | a0001c0002t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28+340A>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324241 | |||||||
| chr1:1324318 | C | G | 1 | a0001c0001t0003g0050 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28+263G>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324318 | |||||||
| chr1:1324351 | T | G | 1 | a0001c0003t0001g0204 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.28+230A>C | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324351 | |||||||
| chr1:1324406 | G | A | 1 | a0001c0002t0001g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.28+175C>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324406 | |||||||
| chr1:1324567 | C | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
7 | HG02735.hp1 HG02735.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+14G>T | INTS11 | ENSG00000127054.22 | transcript | ENST00000435064.6 | protein_coding | 1/16 | chr1 | 1324567 |