Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58493 |
| ensemblid | ENSG00000148153.14 |
| hgncid | 24994 |
| symbol | INIP |
| name | INTS3 and NABP interacting protein |
| refseq_nuc | NM_021218.3 |
| refseq_prot | NP_067041.1 |
| ensembl_nuc | ENST00000374242.9 |
| ensembl_prot | ENSP00000363360.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 112683926 |
| end | 112718117 |
| strand | - |
| ver | v1.2 |
| region | chr9:112683926-112718117 |
| region5000 | chr9:112678926-112723117 |
| regionname0 | INIP_chr9_112683926_112718117 |
| regionname5000 | INIP_chr9_112678926_112723117 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 312 | 372 | 82 | 70 | 166 | 14 | 38 | INIP_chr9_112678926_112723117 | INIP | ATGGC others(307): Show |
chr9 | 112678926 | 112723117 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4114 | 219 | 36 | 45 | 110 | 3 | 24 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0002 | 0/0 | 4118 | 55 | 3 | 15 | 31 | 2 | 4 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0003 | 0/1 | 4115 | 24 | 0 | 3 | 12 | 2 | 6 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0004 | 0/0 | 4118 | 12 | 6 | 1 | 0 | 2 | 3 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0005 | 0/0 | 4115 | 6 | 5 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0006 | 0/0 | 4113 | 6 | 2 | 1 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4108): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0007 | 0/0 | 4118 | 4 | 4 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0008 | 0/0 | 4111 | 4 | 4 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4106): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0009 | 0/0 | 4114 | 4 | 0 | 0 | 4 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0010 | 0/0 | 4117 | 4 | 0 | 0 | 2 | 2 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4112): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0011 | 0/0 | 4114 | 3 | 3 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0012 | 0/0 | 4111 | 3 | 0 | 2 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4106): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0013 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0014 | 0/0 | 4111 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4106): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0015 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0016 | 0/0 | 4114 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0017 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0018 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0019 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0020 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0021 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0022 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0023 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0024 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4112): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0025 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4110): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0026 | 0/0 | 4114 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0027 | 0/0 | 4111 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4106): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0028 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0029 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0030 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0031 | 0/0 | 4117 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4112): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0032 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0033 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0034 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4113): Show |
chr9 | 112678926 | 112723117 |
| a0001c0001t0035 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | AGGAG others(4109): Show |
chr9 | 112678926 | 112723117 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 5 | 3 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0006 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0001 | 0/0 | 12 | 1 | 4 | 4 | 1 | 2 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0007g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0009g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0010g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0012g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0013g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0014g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0015g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0016g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0018g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0020g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0021g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0022g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0023g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0024g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0025g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0026g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0027g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0028g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0029g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0030g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0031g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0032g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0033g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0034g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| a0001c0001t0035g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0095 | EUR | GBR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0173 | EUR | GBR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00280 | hp1 | a0001 | c0001 | t0029 | g0178 | EUR | FIN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0098 | EUR | FIN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | FIN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0086 | EUR | FIN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01069 | hp1 | a0001 | c0001 | t0031 | g0177 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0109 | EUR | IBS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0172 | EUR | IBS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01517 | hp1 | a0001 | c0001 | t0024 | g0174 | EUR | IBS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0117 | EUR | IBS | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01952 | hp1 | a0001 | c0001 | t0018 | g0049 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02004 | hp2 | a0001 | c0001 | t0012 | g0026 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0026 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0134 | EAS | CDX | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02257 | hp1 | a0001 | c0001 | t0019 | g0052 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0068 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02280 | hp1 | a0001 | c0001 | t0034 | g0273 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0170 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0237 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0192 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02630 | hp2 | a0001 | c0001 | t0021 | g0262 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0169 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0091 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0070 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03098 | hp2 | a0001 | c0001 | t0030 | g0065 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03139 | hp1 | a0001 | c0001 | t0035 | g0272 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0062 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0067 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0035 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0137 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | MSL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03834 | hp1 | a0001 | c0001 | t0026 | g0156 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | STU | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0036 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18947 | hp1 | a0001 | c0001 | t0032 | g0250 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18947 | hp2 | a0001 | c0001 | t0020 | g0243 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18997 | hp1 | a0001 | c0001 | t0028 | g0054 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19003 | hp1 | a0001 | c0001 | t0027 | g0063 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0168 | AFR | LWK | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19078 | hp1 | a0001 | c0001 | t0009 | g0269 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0118 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA19240 | hp2 | a0001 | c0001 | t0033 | g0271 | AFR | YRI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ASW | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ASW | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0267 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0036 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0247 | AFR | USA | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0094 | REF | REF | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0190 | REF | REF | INIP_chr9_112678926_112723117 | INIP | chr9 | 112678926 | 112723117 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112683968 | T | TCATA | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3569_*3570insTATG | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 3569 | chr9 | 112683968 | ||||||
| chr9:112684146 | C | T | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(1): Show |
62 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3392G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 3392 | chr9 | 112684146 | ||||||
| chr9:112684206 | C | T | 1 | a0001c0001t0009 | 4 | NA18974.hp2 NA18975.hp1 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3332G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 3332 | chr9 | 112684206 | ||||||
| chr9:112684389 | A | T | 1 | a0001c0001t0013 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3149T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 3149 | chr9 | 112684389 | ||||||
| chr9:112684592 | C | T | 1 | a0001c0001t0013 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2946G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2946 | chr9 | 112684592 | ||||||
| chr9:112684596 | C | T | 1 | a0001c0001t0028 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2942G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2942 | chr9 | 112684596 | ||||||
| chr9:112684685 | A | T | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(1): Show |
62 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2853T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2853 | chr9 | 112684685 | ||||||
| chr9:112685000 | C | G | 1 | a0001c0001t0016 | 2 | HG02486.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2538G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2538 | chr9 | 112685000 | ||||||
| chr9:112685041 | G | T | 1 | a0001c0001t0015 | 2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2497C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2497 | chr9 | 112685041 | ||||||
| chr9:112685202 | C | T | 4 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0029 others(1): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2336G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2336 | chr9 | 112685202 | ||||||
| chr9:112685238 | T | C | 1 | a0001c0001t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2300A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2300 | chr9 | 112685238 | ||||||
| chr9:112685246 | CT | C | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0024 others(1): Show |
12 | HG01069.hp1 HG01168.hp2 HG01515.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2291delA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2291 | chr9 | 112685246 | ||||||
| chr9:112685284 | G | T | 1 | a0001c0001t0028 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2254C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2254 | chr9 | 112685284 | ||||||
| chr9:112685299 | C | T | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0022 |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2239G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2239 | chr9 | 112685299 | ||||||
| chr9:112685495 | G | A | 1 | a0001c0001t0017 | 2 | HG03486.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2043C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2043 | chr9 | 112685495 | ||||||
| chr9:112685529 | AAAG | A | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(8): Show |
46 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2006_*2008delCTT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 2006 | chr9 | 112685529 | ||||||
| chr9:112685655 | T | C | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(13): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1883A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1883 | chr9 | 112685655 | ||||||
| chr9:112685681 | G | T | 2 | a0001c0001t0008 a0001c0001t0014 |
6 | HG02615.hp1 HG02886.hp2 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1857C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1857 | chr9 | 112685681 | ||||||
| chr9:112685684 | A | T | 2 | a0001c0001t0008 a0001c0001t0014 |
6 | HG02615.hp1 HG02886.hp2 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1854T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1854 | chr9 | 112685684 | ||||||
| chr9:112685887 | A | G | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(11): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1651T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1651 | chr9 | 112685887 | ||||||
| chr9:112685890 | G | T | 1 | a0001c0001t0023 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1648 | chr9 | 112685890 | ||||||
| chr9:112685915 | A | C | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0021 others(3): Show |
20 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1623T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1623 | chr9 | 112685915 | ||||||
| chr9:112686061 | T | G | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0021 others(3): Show |
20 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1477A>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1477 | chr9 | 112686061 | ||||||
| chr9:112686285 | A | C | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02818.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1253T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1253 | chr9 | 112686285 | ||||||
| chr9:112686409 | G | C | 1 | a0001c0001t0032 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 1129 | chr9 | 112686409 | ||||||
| chr9:112686599 | C | T | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(7): Show |
30 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 939 | chr9 | 112686599 | ||||||
| chr9:112686637 | C | T | 1 | a0001c0001t0014 | 2 | HG03139.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*901G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 901 | chr9 | 112686637 | ||||||
| chr9:112686830 | C | T | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(7): Show |
30 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*708G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 708 | chr9 | 112686830 | ||||||
| chr9:112686840 | C | T | 1 | a0001c0001t0021 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*698G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 698 | chr9 | 112686840 | ||||||
| chr9:112687190 | A | G | 1 | a0001c0001t0026 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 348 | chr9 | 112687190 | ||||||
| chr9:112687276 | C | G | 14 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(11): Show |
39 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*262G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 262 | chr9 | 112687276 | ||||||
| chr9:112687283 | A | T | 1 | a0001c0001t0020 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 5/5 | 255 | chr9 | 112687283 | ||||||
| chr9:112718060 | A | G | 2 | a0001c0001t0005 a0001c0001t0019 |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-130T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/5 | chr9 | 112718060 | |||||||
| chr9:112718061 | G | A | 1 | a0001c0001t0033 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/5 | 1576 | chr9 | 112718061 | ||||||
| chr9:112718066 | G | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02280.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-136C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/5 | 1581 | chr9 | 112718066 | ||||||
| chr9:112718070 | A | G | 1 | a0001c0001t0018 | 1 | HG01952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/5 | 1585 | chr9 | 112718070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112687692 | G | A | 4 | a0001c0001t0007g0045 a0001c0001t0007g0236 a0001c0001t0007g0247 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-59C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687692 | |||||||
| chr9:112687807 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0037 others(45): Show |
63 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.220-174A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687807 | |||||||
| chr9:112687813 | C | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.220-180G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687813 | |||||||
| chr9:112687814 | G | A | 1 | a0001c0001t0004g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220-181C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687814 | |||||||
| chr9:112687827 | G | T | 1 | a0001c0001t0030g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220-194C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687827 | |||||||
| chr9:112687856 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.220-223A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687856 | |||||||
| chr9:112687860 | C | T | 5 | a0001c0001t0001g0165 a0001c0001t0008g0022 a0001c0001t0008g0069 others(2): Show |
7 | HG02615.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-227G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687860 | |||||||
| chr9:112687861 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.220-228C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687861 | |||||||
| chr9:112687881 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | NA19011.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.220-248G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687881 | |||||||
| chr9:112687882 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.220-249C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687882 | |||||||
| chr9:112687890 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0005g0051 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.220-257G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687890 | |||||||
| chr9:112687912 | C | T | 32 | a0001c0001t0004g0127 a0001c0001t0004g0146 a0001c0001t0004g0171 others(29): Show |
36 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.220-279G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687912 | |||||||
| chr9:112687943 | A | G | 26 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0132 others(23): Show |
29 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.220-310T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112687943 | |||||||
| chr9:112688073 | G | A | 17 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0086 others(14): Show |
21 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-440C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688073 | |||||||
| chr9:112688081 | A | G | 34 | a0001c0001t0004g0127 a0001c0001t0004g0146 a0001c0001t0004g0171 others(31): Show |
39 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-448T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688081 | |||||||
| chr9:112688085 | C | CAAAT | 97 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0038 others(94): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.220-456_220-453dup others(4): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688085 | |||||||
| chr9:112688085 | C | CAAATAAA others(1): Show |
20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0047 others(17): Show |
31 | HG00423.hp1 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.220-460_220-453dup others(8): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688085 | |||||||
| chr9:112688085 | C | CAAATAAA others(5): Show |
8 | a0001c0001t0001g0046 a0001c0001t0003g0086 a0001c0001t0005g0050 others(5): Show |
9 | HG00323.hp2 HG02486.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-464_220-453dup others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688085 | |||||||
| chr9:112688085 | CAAATAAA others(1): Show |
C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0016g0036 |
4 | HG01243.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-460_220-453del others(8): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688085 | |||||||
| chr9:112688085 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-464_220-453del others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688085 | |||||||
| chr9:112688284 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.220-651A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688284 | |||||||
| chr9:112688385 | G | C | 1 | a0001c0001t0027g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.220-752C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688385 | |||||||
| chr9:112688422 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0197 |
2 | NA18989.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.220-789T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688422 | |||||||
| chr9:112688489 | TA | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0087 a0001c0001t0001g0111 others(26): Show |
38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.220-857delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688489 | |||||||
| chr9:112688489 | TAA | T | 4 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0132 others(1): Show |
6 | HG02602.hp2 HG03669.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-858_220-857del others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688489 | |||||||
| chr9:112688625 | A | G | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.219+902T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688625 | |||||||
| chr9:112688740 | G | A | 1 | a0001c0001t0004g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.219+787C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688740 | |||||||
| chr9:112688829 | C | T | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.219+698G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688829 | |||||||
| chr9:112688874 | G | A | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.219+653C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688874 | |||||||
| chr9:112688950 | G | GA | 15 | a0001c0001t0004g0127 a0001c0001t0004g0146 a0001c0001t0004g0171 others(12): Show |
15 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+576_219+577ins others(1): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688950 | |||||||
| chr9:112688951 | G | A | 34 | a0001c0001t0004g0127 a0001c0001t0004g0146 a0001c0001t0004g0171 others(31): Show |
39 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.219+576C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688951 | |||||||
| chr9:112688959 | T | C | 55 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(52): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.219+568A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112688959 | |||||||
| chr9:112689116 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.219+411C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112689116 | |||||||
| chr9:112689520 | T | C | 2 | a0001c0001t0001g0257 a0001c0001t0023g0170 |
2 | HG02451.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.219+7A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 4/4 | chr9 | 112689520 | |||||||
| chr9:112689730 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.129-113G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112689730 | |||||||
| chr9:112689833 | A | AC | 4 | a0001c0001t0003g0025 a0001c0001t0003g0097 a0001c0001t0003g0101 others(1): Show |
5 | HG00544.hp2 HG02135.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-217_129-216ins others(1): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112689833 | |||||||
| chr9:112690006 | T | C | 21 | a0001c0001t0001g0263 a0001c0001t0004g0127 a0001c0001t0004g0146 others(18): Show |
23 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.129-389A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690006 | |||||||
| chr9:112690015 | A | C | 5 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-398T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690015 | |||||||
| chr9:112690076 | CTA | C | 21 | a0001c0001t0001g0263 a0001c0001t0004g0127 a0001c0001t0004g0146 others(18): Show |
23 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.129-461_129-460del others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690076 | |||||||
| chr9:112690179 | G | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0012 others(31): Show |
59 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.129-562C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690179 | |||||||
| chr9:112690376 | A | G | 15 | a0001c0001t0001g0263 a0001c0001t0004g0127 a0001c0001t0004g0146 others(12): Show |
15 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.129-759T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690376 | |||||||
| chr9:112690377 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
36 | HG00423.hp1 HG00621.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.129-760G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690377 | |||||||
| chr9:112690385 | G | C | 21 | a0001c0001t0001g0263 a0001c0001t0004g0127 a0001c0001t0004g0146 others(18): Show |
23 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.129-768C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690385 | |||||||
| chr9:112690411 | TG | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0016g0036 |
4 | HG01243.hp2 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-795delC | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690411 | |||||||
| chr9:112690472 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
39 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.129-855G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690472 | |||||||
| chr9:112690478 | A | G | 1 | a0001c0001t0004g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129-861T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690478 | |||||||
| chr9:112690522 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.129-905G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690522 | |||||||
| chr9:112690629 | C | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(43): Show |
62 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.129-1012G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690629 | |||||||
| chr9:112690710 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.129-1093T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690710 | |||||||
| chr9:112690744 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0268 |
3 | HG02145.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-1127C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690744 | |||||||
| chr9:112690813 | C | T | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.129-1196G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690813 | |||||||
| chr9:112690968 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0212 |
2 | HG01192.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.129-1351A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112690968 | |||||||
| chr9:112691031 | C | T | 1 | a0001c0001t0014g0035 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129-1414G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691031 | |||||||
| chr9:112691204 | T | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(54): Show |
75 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.129-1587A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691204 | |||||||
| chr9:112691458 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.129-1841C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691458 | |||||||
| chr9:112691486 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.129-1869C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691486 | |||||||
| chr9:112691503 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129-1886G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691503 | |||||||
| chr9:112691623 | C | T | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-2006G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691623 | |||||||
| chr9:112691646 | G | C | 1 | a0001c0001t0003g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.129-2029C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691646 | |||||||
| chr9:112691883 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.128+2248C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112691883 | |||||||
| chr9:112692022 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128+2109C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692022 | |||||||
| chr9:112692023 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0249 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.128+2095_128+2107d others(15): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692023 | |||||||
| chr9:112692032 | AAAAG | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
38 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.128+2095_128+2098d others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692032 | |||||||
| chr9:112692062 | T | C | 2 | a0001c0001t0008g0022 a0001c0001t0008g0069 |
3 | HG02886.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.128+2069A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692062 | |||||||
| chr9:112692097 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
39 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.128+2034A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692097 | |||||||
| chr9:112692142 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.128+1989T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692142 | |||||||
| chr9:112692181 | C | T | 113 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(110): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.128+1950G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692181 | |||||||
| chr9:112692224 | C | A | 79 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+1907G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692224 | |||||||
| chr9:112692278 | G | A | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(6): Show |
11 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.128+1853C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692278 | |||||||
| chr9:112692338 | T | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
55 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.128+1793A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692338 | |||||||
| chr9:112692503 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.128+1628G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692503 | |||||||
| chr9:112692581 | G | T | 1 | a0001c0001t0001g0017 | 3 | HG01069.hp2 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.128+1550C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692581 | |||||||
| chr9:112692734 | C | CA | 8 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0176 others(5): Show |
8 | HG01515.hp2 HG01517.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+1396dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692734 | |||||||
| chr9:112692889 | A | AC | 17 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0086 others(14): Show |
21 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.128+1241_128+1242i others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692889 | |||||||
| chr9:112692902 | A | G | 79 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+1229T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692902 | |||||||
| chr9:112692946 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.128+1185G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112692946 | |||||||
| chr9:112693028 | C | CA | 47 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0087 others(44): Show |
58 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.128+1102dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693028 | |||||||
| chr9:112693028 | C | CAAA | 4 | a0001c0001t0005g0009 a0001c0001t0005g0051 a0001c0001t0019g0052 others(1): Show |
6 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+1100_128+1102d others(5): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693028 | |||||||
| chr9:112693028 | C | CAAAA | 18 | a0001c0001t0001g0263 a0001c0001t0004g0127 a0001c0001t0004g0146 others(15): Show |
18 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.128+1099_128+1102d others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693028 | |||||||
| chr9:112693028 | CA | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0163 a0001c0001t0001g0176 others(9): Show |
15 | HG01167.hp1 HG01884.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.128+1102delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693028 | |||||||
| chr9:112693466 | C | A | 6 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 others(3): Show |
8 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+665G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693466 | |||||||
| chr9:112693468 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128+663G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693468 | |||||||
| chr9:112693472 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128+659A>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693472 | |||||||
| chr9:112693473 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128+658C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112693473 | |||||||
| chr9:112694070 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0013g0192 others(1): Show |
5 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+61C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112694070 | |||||||
| chr9:112694073 | TCAAAA | T | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+53_128+57delTT others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112694073 | |||||||
| chr9:112694073 | TCAAAACA others(3): Show |
T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.128+48_128+57delTT others(8): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 3/4 | chr9 | 112694073 | |||||||
| chr9:112694264 | G | GAGAA | 8 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(5): Show |
10 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-35_26-32dupTTCT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694264 | |||||||
| chr9:112694317 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.26-84T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694317 | |||||||
| chr9:112694329 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-96C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694329 | |||||||
| chr9:112694618 | G | A | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.26-385C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694618 | |||||||
| chr9:112694622 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-389T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694622 | |||||||
| chr9:112694719 | A | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.26-486T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694719 | |||||||
| chr9:112694771 | A | C | 1 | a0001c0001t0025g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-538T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694771 | |||||||
| chr9:112694837 | C | G | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-604G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112694837 | |||||||
| chr9:112695255 | G | GA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0001g0196 others(3): Show |
7 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-1023dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695255 | |||||||
| chr9:112695255 | GA | G | 56 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0001g0155 others(53): Show |
88 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-1023delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695255 | |||||||
| chr9:112695256 | A | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0102 a0001c0001t0003g0103 |
3 | HG00639.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.26-1023T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695256 | |||||||
| chr9:112695379 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0012 others(31): Show |
59 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.26-1146C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695379 | |||||||
| chr9:112695576 | T | G | 43 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
57 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.26-1343A>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695576 | |||||||
| chr9:112695720 | A | T | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(6): Show |
11 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-1487T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695720 | |||||||
| chr9:112695725 | A | AGAAGAAG others(26): Show |
1 | a0001c0001t0002g0119 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.26-1525_26-1493dup others(33): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695725 | |||||||
| chr9:112695776 | AGGAGGG | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
35 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-1549_26-1544del others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695776 | |||||||
| chr9:112695794 | GGGA | G | 11 | a0001c0001t0001g0032 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
13 | HG00323.hp1 HG00738.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-1564_26-1562del others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695794 | |||||||
| chr9:112695794 | GGGAGGA | G | 5 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 others(2): Show |
7 | HG02615.hp1 HG02886.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-1567_26-1562del others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695794 | |||||||
| chr9:112695800 | A | G | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0015g0067 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-1567T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695800 | |||||||
| chr9:112695805 | GAGGAGAA others(5): Show |
G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(52): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.26-1584_26-1573del others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695805 | |||||||
| chr9:112695808 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0228 |
2 | NA18985.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.26-1575C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695808 | |||||||
| chr9:112695811 | A | AAGAAGGA others(11): Show |
1 | a0001c0001t0001g0228 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.26-1579_26-1578ins others(18): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695811 | |||||||
| chr9:112695811 | A | AAGAAGGA others(20): Show |
1 | a0001c0001t0001g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.26-1579_26-1578ins others(27): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695811 | |||||||
| chr9:112695811 | A | G | 23 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(20): Show |
25 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-1578T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695811 | |||||||
| chr9:112695820 | GAGAAGAA others(17): Show |
G | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-1611_26-1588del others(24): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695820 | |||||||
| chr9:112695826 | AAGAAGGA others(8): Show |
A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-1608_26-1594del others(15): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695826 | |||||||
| chr9:112695832 | GAGAAGAA others(5): Show |
G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0019 others(58): Show |
79 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.26-1611_26-1600del others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695832 | |||||||
| chr9:112695844 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-1611T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695844 | |||||||
| chr9:112695946 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.26-1713C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112695946 | |||||||
| chr9:112696114 | A | G | 1 | a0001c0001t0010g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.26-1881T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696114 | |||||||
| chr9:112696179 | A | T | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(6): Show |
11 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-1946T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696179 | |||||||
| chr9:112696181 | T | C | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-1948A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696181 | |||||||
| chr9:112696223 | G | A | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.26-1990C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696223 | |||||||
| chr9:112696279 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
35 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-2046G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696279 | |||||||
| chr9:112696349 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
77 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.26-2116A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696349 | |||||||
| chr9:112696351 | G | T | 1 | a0001c0001t0030g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.26-2118C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696351 | |||||||
| chr9:112696378 | G | A | 5 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-2145C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696378 | |||||||
| chr9:112696404 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0199 |
2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.26-2171C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696404 | |||||||
| chr9:112696609 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-2376T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696609 | |||||||
| chr9:112696648 | G | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
39 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.26-2415C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696648 | |||||||
| chr9:112696866 | C | T | 1 | a0001c0001t0004g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.26-2633G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696866 | |||||||
| chr9:112696882 | G | A | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-2649C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696882 | |||||||
| chr9:112696908 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.26-2675G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112696908 | |||||||
| chr9:112697072 | C | A | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-2839G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697072 | |||||||
| chr9:112697362 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0144 others(2): Show |
8 | HG00099.hp2 HG00733.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-3129G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697362 | |||||||
| chr9:112697428 | A | G | 23 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(20): Show |
25 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-3195T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697428 | |||||||
| chr9:112697529 | G | A | 7 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 others(4): Show |
9 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-3296C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697529 | |||||||
| chr9:112697576 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG01069.hp2 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.26-3343G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697576 | |||||||
| chr9:112697632 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.26-3399G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697632 | |||||||
| chr9:112697653 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.26-3420T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697653 | |||||||
| chr9:112697814 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.26-3581T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697814 | |||||||
| chr9:112697959 | G | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
77 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.26-3726C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112697959 | |||||||
| chr9:112698000 | T | C | 4 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0132 others(1): Show |
6 | HG02602.hp2 HG03669.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-3767A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698000 | |||||||
| chr9:112698032 | C | T | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.26-3799G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698032 | |||||||
| chr9:112698173 | G | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(47): Show |
66 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.26-3940C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698173 | |||||||
| chr9:112698242 | T | A | 4 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 others(1): Show |
6 | HG02615.hp1 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4009A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698242 | |||||||
| chr9:112698303 | C | CA | 46 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0071 others(43): Show |
66 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.26-4071dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698303 | |||||||
| chr9:112698303 | C | CAA | 27 | a0001c0001t0001g0241 a0001c0001t0002g0005 a0001c0001t0002g0107 others(24): Show |
37 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.26-4072_26-4071dup others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698303 | |||||||
| chr9:112698303 | C | CAAA | 10 | a0001c0001t0002g0012 a0001c0001t0002g0104 a0001c0001t0002g0121 others(7): Show |
13 | HG00099.hp1 HG00544.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-4073_26-4071dup others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698303 | |||||||
| chr9:112698303 | CA | C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(32): Show |
50 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.26-4071delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698303 | |||||||
| chr9:112698344 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.26-4111C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698344 | |||||||
| chr9:112698352 | T | C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-4119A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698352 | |||||||
| chr9:112698412 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-4179C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698412 | |||||||
| chr9:112698510 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-4277A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112698510 | |||||||
| chr9:112699029 | A | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | NA19000.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.26-4796T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699029 | |||||||
| chr9:112699034 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.26-4801G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699034 | |||||||
| chr9:112699348 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.26-5115A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699348 | |||||||
| chr9:112699537 | T | C | 1 | a0001c0001t0001g0020 | 3 | NA18959.hp1 NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.26-5304A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699537 | |||||||
| chr9:112699584 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.26-5351C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699584 | |||||||
| chr9:112699598 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.26-5365T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699598 | |||||||
| chr9:112699741 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-5508C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699741 | |||||||
| chr9:112699767 | G | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
35 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-5534C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699767 | |||||||
| chr9:112699812 | T | A | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(6): Show |
11 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-5579A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699812 | |||||||
| chr9:112699840 | A | C | 3 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 |
4 | HG02615.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-5607T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112699840 | |||||||
| chr9:112700272 | T | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(45): Show |
64 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.26-6039A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700272 | |||||||
| chr9:112700314 | A | G | 23 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(20): Show |
25 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-6081T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700314 | |||||||
| chr9:112700330 | C | T | 6 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0268 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-6097G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700330 | |||||||
| chr9:112700360 | A | AGGCCCCT others(15): Show |
1 | a0001c0001t0001g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.26-6149_26-6128dup others(22): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700360 | |||||||
| chr9:112700365 | C | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
77 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.26-6132G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700365 | |||||||
| chr9:112700491 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26-6258T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700491 | |||||||
| chr9:112700518 | A | ATATAT | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-6290_26-6286dup others(5): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700518 | |||||||
| chr9:112700524 | A | AAT | 2 | a0001c0001t0001g0040 a0001c0001t0006g0202 |
3 | NA18954.hp2 NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.26-6293_26-6292dup others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700524 | |||||||
| chr9:112700531 | ATATATAT | A | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(4): Show |
9 | HG01884.hp2 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-6305_26-6299del others(7): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700531 | |||||||
| chr9:112700537 | AT | A | 14 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(11): Show |
14 | HG01106.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.26-6305delA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700537 | |||||||
| chr9:112700538 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.26-6305A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700538 | |||||||
| chr9:112700538 | T | TA | 27 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
39 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.26-6306_26-6305ins others(1): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700538 | |||||||
| chr9:112700538 | T | TATA | 4 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0005g0051 others(1): Show |
5 | HG03540.hp1 NA18950.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-6306_26-6305ins others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700538 | |||||||
| chr9:112700538 | T | TATATATA | 3 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0053 |
4 | HG01109.hp2 HG02486.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-6306_26-6305ins others(7): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700538 | |||||||
| chr9:112700592 | C | T | 1 | a0001c0001t0025g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-6359G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700592 | |||||||
| chr9:112700596 | A | G | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-6363T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700596 | |||||||
| chr9:112700669 | T | A | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-6436A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700669 | |||||||
| chr9:112700721 | T | A | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(14): Show |
17 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-6488A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700721 | |||||||
| chr9:112700809 | A | G | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(6): Show |
11 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-6576T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700809 | |||||||
| chr9:112700812 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0059 others(2): Show |
7 | NA18612.hp1 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-6579C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700812 | |||||||
| chr9:112700920 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0147 a0001c0001t0001g0238 |
4 | NA18952.hp1 NA18978.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-6687G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112700920 | |||||||
| chr9:112701042 | C | T | 1 | a0001c0001t0004g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-6809G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701042 | |||||||
| chr9:112701061 | C | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0097 a0001c0001t0003g0101 others(1): Show |
5 | HG00544.hp2 HG02135.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-6828G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701061 | |||||||
| chr9:112701497 | A | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(77): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.26-7264T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701497 | |||||||
| chr9:112701504 | G | A | 1 | a0001c0001t0025g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-7271C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701504 | |||||||
| chr9:112701716 | G | T | 1 | a0001c0001t0015g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-7483C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701716 | |||||||
| chr9:112701899 | A | T | 1 | a0001c0001t0015g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.26-7666T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701899 | |||||||
| chr9:112701900 | A | T | 48 | a0001c0001t0001g0181 a0001c0001t0001g0212 a0001c0001t0001g0260 others(45): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-7667T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701900 | |||||||
| chr9:112701901 | T | A | 35 | a0001c0001t0001g0079 a0001c0001t0002g0001 a0001c0001t0002g0005 others(32): Show |
60 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.26-7668A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701901 | |||||||
| chr9:112701902 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.26-7669A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112701902 | |||||||
| chr9:112702194 | G | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
77 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.26-7961C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702194 | |||||||
| chr9:112702213 | T | C | 3 | a0001c0001t0008g0022 a0001c0001t0008g0069 a0001c0001t0008g0237 |
4 | HG02615.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-7980A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702213 | |||||||
| chr9:112702345 | T | C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-8112A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702345 | |||||||
| chr9:112702551 | G | A | 8 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0008g0022 others(5): Show |
10 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-8318C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702551 | |||||||
| chr9:112702588 | C | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0085 others(7): Show |
11 | HG01175.hp2 HG01243.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-8355G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702588 | |||||||
| chr9:112702689 | C | G | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-8456G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702689 | |||||||
| chr9:112702717 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(171): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.26-8484T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702717 | |||||||
| chr9:112702754 | G | A | 1 | a0001c0001t0001g0020 | 3 | NA18959.hp1 NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.26-8521C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702754 | |||||||
| chr9:112702850 | A | G | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-8617T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702850 | |||||||
| chr9:112702856 | C | T | 2 | a0001c0001t0007g0045 a0001c0001t0007g0236 |
3 | HG02109.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26-8623G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112702856 | |||||||
| chr9:112703002 | A | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
56 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-8769T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703002 | |||||||
| chr9:112703157 | A | G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.26-8924T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703157 | |||||||
| chr9:112703310 | C | G | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-9077G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703310 | |||||||
| chr9:112703540 | G | A | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-9307C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703540 | |||||||
| chr9:112703589 | G | C | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0015g0067 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-9356C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703589 | |||||||
| chr9:112703697 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.26-9464G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703697 | |||||||
| chr9:112703877 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.26-9644C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112703877 | |||||||
| chr9:112704071 | T | C | 3 | a0001c0001t0015g0067 a0001c0001t0015g0068 a0001c0001t0025g0070 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-9838A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704071 | |||||||
| chr9:112704091 | G | T | 1 | a0001c0001t0003g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.26-9858C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704091 | |||||||
| chr9:112704232 | T | A | 6 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
8 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-9999A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704232 | |||||||
| chr9:112704270 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-10037C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704270 | |||||||
| chr9:112704413 | A | C | 1 | a0001c0001t0023g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-10180T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704413 | |||||||
| chr9:112704527 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.26-10294A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704527 | |||||||
| chr9:112704629 | A | G | 1 | a0001c0001t0008g0237 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.26-10396T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704629 | |||||||
| chr9:112704677 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
34 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.26-10444G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704677 | |||||||
| chr9:112704760 | G | GA | 28 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0003g0011 others(25): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.26-10528dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112704760 | |||||||
| chr9:112705110 | C | CA | 53 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0024 others(50): Show |
64 | HG00140.hp2 HG00423.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.26-10878dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705110 | |||||||
| chr9:112705110 | C | CAA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
10 | HG01884.hp2 HG02135.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-10879_26-10878d others(4): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705110 | |||||||
| chr9:112705110 | CA | C | 46 | a0001c0001t0001g0057 a0001c0001t0001g0227 a0001c0001t0002g0001 others(43): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.26-10878delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705110 | |||||||
| chr9:112705273 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.26-11040A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705273 | |||||||
| chr9:112705319 | T | A | 35 | a0001c0001t0001g0217 a0001c0001t0002g0001 a0001c0001t0002g0005 others(32): Show |
60 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.26-11086A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705319 | |||||||
| chr9:112705348 | G | A | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.25+11113C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705348 | |||||||
| chr9:112705404 | G | A | 3 | a0001c0001t0015g0067 a0001c0001t0015g0068 a0001c0001t0025g0070 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+11057C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705404 | |||||||
| chr9:112705502 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.25+10959C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705502 | |||||||
| chr9:112705620 | A | T | 2 | a0001c0001t0001g0040 a0001c0001t0006g0202 |
3 | NA18954.hp2 NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.25+10841T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705620 | |||||||
| chr9:112705720 | A | G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+10741T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705720 | |||||||
| chr9:112705988 | G | C | 4 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+10473C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112705988 | |||||||
| chr9:112706008 | A | G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+10453T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706008 | |||||||
| chr9:112706045 | C | G | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+10416G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706045 | |||||||
| chr9:112706093 | GA | G | 4 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+10367delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706093 | |||||||
| chr9:112706290 | T | C | 2 | a0001c0001t0008g0022 a0001c0001t0008g0069 |
3 | HG02886.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.25+10171A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706290 | |||||||
| chr9:112706352 | G | A | 3 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 |
3 | HG02258.hp2 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.25+10109C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706352 | |||||||
| chr9:112706356 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0131 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.25+10105G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706356 | |||||||
| chr9:112706495 | C | G | 1 | a0001c0001t0022g0091 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25+9966G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706495 | |||||||
| chr9:112706717 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.25+9744T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706717 | |||||||
| chr9:112706933 | T | C | 3 | a0001c0001t0015g0067 a0001c0001t0015g0068 a0001c0001t0025g0070 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+9528A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706933 | |||||||
| chr9:112706951 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.25+9510C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112706951 | |||||||
| chr9:112707059 | G | T | 5 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+9402C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707059 | |||||||
| chr9:112707081 | AC | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02056.hp2 NA18953.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.25+9379delG | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707081 | |||||||
| chr9:112707153 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0009g0018 a0001c0001t0009g0269 |
7 | HG02135.hp1 NA18954.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+9308C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707153 | |||||||
| chr9:112707240 | C | CT | 5 | a0001c0001t0001g0176 a0001c0001t0001g0244 a0001c0001t0002g0108 others(2): Show |
6 | HG01346.hp1 HG01515.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+9220dupA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707240 | |||||||
| chr9:112707240 | CT | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0001g0145 others(12): Show |
15 | HG00639.hp1 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.25+9220delA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707240 | |||||||
| chr9:112707330 | CT | C | 6 | a0001c0001t0001g0198 a0001c0001t0001g0226 a0001c0001t0004g0259 others(3): Show |
7 | HG02258.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+9130delA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707330 | |||||||
| chr9:112707484 | GTTTCTTT others(16): Show |
G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+8954_25+8976del others(23): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707484 | |||||||
| chr9:112707503 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+8958C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112707503 | |||||||
| chr9:112708100 | G | T | 1 | a0001c0001t0003g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.25+8361C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708100 | |||||||
| chr9:112708144 | A | G | 3 | a0001c0001t0015g0067 a0001c0001t0015g0068 a0001c0001t0025g0070 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+8317T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708144 | |||||||
| chr9:112708181 | G | T | 1 | a0001c0001t0030g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.25+8280C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708181 | |||||||
| chr9:112708217 | C | T | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0013g0062 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+8244G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708217 | |||||||
| chr9:112708303 | A | G | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+8158T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708303 | |||||||
| chr9:112708393 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.25+8068C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708393 | |||||||
| chr9:112708455 | A | G | 1 | a0001c0001t0015g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25+8006T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708455 | |||||||
| chr9:112708492 | A | T | 10 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+7969T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708492 | |||||||
| chr9:112708616 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0268 |
3 | HG02145.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+7845G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708616 | |||||||
| chr9:112708652 | G | C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+7809C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708652 | |||||||
| chr9:112708706 | A | AT | 7 | a0001c0001t0004g0146 a0001c0001t0004g0171 a0001c0001t0004g0172 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7754dupA | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708706 | |||||||
| chr9:112708751 | C | T | 1 | a0001c0001t0012g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.25+7710G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708751 | |||||||
| chr9:112708845 | C | CTT | 9 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG02145.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+7614_25+7615dup others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708845 | |||||||
| chr9:112708965 | TACTC | T | 1 | a0001c0001t0001g0020 | 3 | NA18959.hp1 NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.25+7492_25+7495del others(4): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112708965 | |||||||
| chr9:112709017 | A | T | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+7444T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709017 | |||||||
| chr9:112709042 | C | G | 36 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0002g0001 others(33): Show |
61 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.25+7419G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709042 | |||||||
| chr9:112709066 | T | C | 7 | a0001c0001t0004g0146 a0001c0001t0004g0171 a0001c0001t0004g0172 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7395A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709066 | |||||||
| chr9:112709251 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
35 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.25+7210A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709251 | |||||||
| chr9:112709402 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.25+7059G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709402 | |||||||
| chr9:112709453 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(115): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.25+7008G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709453 | |||||||
| chr9:112709950 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(115): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.25+6511C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112709950 | |||||||
| chr9:112710003 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0059 others(2): Show |
7 | NA18612.hp1 NA18946.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+6458A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710003 | |||||||
| chr9:112710407 | C | A | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+6054G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710407 | |||||||
| chr9:112710414 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.25+6047G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710414 | |||||||
| chr9:112710622 | C | T | 1 | a0001c0001t0007g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25+5839G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710622 | |||||||
| chr9:112710686 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+5775C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710686 | |||||||
| chr9:112710727 | T | C | 1 | a0001c0001t0018g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.25+5734A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710727 | |||||||
| chr9:112710758 | A | T | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+5703T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112710758 | |||||||
| chr9:112711027 | A | C | 1 | a0001c0001t0005g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+5434T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711027 | |||||||
| chr9:112711029 | A | G | 2 | a0001c0001t0007g0045 a0001c0001t0007g0236 |
3 | HG02109.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.25+5432T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711029 | |||||||
| chr9:112711061 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.25+5400C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711061 | |||||||
| chr9:112711251 | C | A | 7 | a0001c0001t0004g0146 a0001c0001t0004g0171 a0001c0001t0004g0172 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+5210G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711251 | |||||||
| chr9:112711452 | TTAC | T | 4 | a0001c0001t0001g0263 a0001c0001t0004g0234 a0001c0001t0004g0264 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+5006_25+5008del others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711452 | |||||||
| chr9:112711503 | T | C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+4958A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711503 | |||||||
| chr9:112711545 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+4916A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711545 | |||||||
| chr9:112711561 | A | G | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0013g0062 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+4900T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711561 | |||||||
| chr9:112711680 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0006g0223 |
2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.25+4781C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711680 | |||||||
| chr9:112711707 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0268 |
3 | HG02145.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+4754G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711707 | |||||||
| chr9:112711715 | G | T | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+4746C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711715 | |||||||
| chr9:112711812 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18944.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.25+4649C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711812 | |||||||
| chr9:112711958 | C | T | 4 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+4503G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112711958 | |||||||
| chr9:112712020 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+4441A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712020 | |||||||
| chr9:112712270 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+4191G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712270 | |||||||
| chr9:112712376 | CA | C | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0013g0062 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+4084delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712376 | |||||||
| chr9:112712377 | A | T | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+4084T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712377 | |||||||
| chr9:112712388 | A | T | 2 | a0001c0001t0033g0271 a0001c0001t0035g0272 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.25+4073T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712388 | |||||||
| chr9:112712447 | T | TAAG | 9 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+4011_25+4013dup others(3): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712447 | |||||||
| chr9:112712621 | A | C | 1 | a0001c0001t0008g0237 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.25+3840T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712621 | |||||||
| chr9:112712756 | T | C | 1 | a0001c0001t0014g0035 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.25+3705A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712756 | |||||||
| chr9:112712801 | G | C | 2 | a0001c0001t0001g0266 a0001c0001t0011g0267 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.25+3660C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712801 | |||||||
| chr9:112712986 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.25+3475G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112712986 | |||||||
| chr9:112713015 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+3446C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713015 | |||||||
| chr9:112713317 | C | G | 5 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(2): Show |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+3144G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713317 | |||||||
| chr9:112713334 | G | T | 1 | a0001c0001t0014g0035 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.25+3127C>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713334 | |||||||
| chr9:112713374 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.25+3087T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713374 | |||||||
| chr9:112713376 | A | C | 4 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+3085T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713376 | |||||||
| chr9:112713380 | G | A | 1 | a0001c0001t0001g0017 | 3 | HG01069.hp2 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.25+3081C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713380 | |||||||
| chr9:112713579 | C | G | 4 | a0001c0001t0013g0062 a0001c0001t0015g0067 a0001c0001t0015g0068 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+2882G>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713579 | |||||||
| chr9:112713857 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25+2604C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713857 | |||||||
| chr9:112713984 | C | CA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0227 a0001c0001t0001g0232 others(5): Show |
9 | HG01884.hp2 HG01943.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2476dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713984 | |||||||
| chr9:112713984 | CAAAAAAA | C | 11 | a0001c0001t0005g0009 a0001c0001t0005g0050 a0001c0001t0005g0051 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+2470_25+2476del others(7): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112713984 | |||||||
| chr9:112714034 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.25+2427G>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714034 | |||||||
| chr9:112714044 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+2417G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714044 | |||||||
| chr9:112714073 | A | C | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0029 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.25+2388T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714073 | |||||||
| chr9:112714133 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(78): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.25+2328G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714133 | |||||||
| chr9:112714360 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0086 others(16): Show |
24 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+2101G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714360 | |||||||
| chr9:112714452 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.25+2009T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714452 | |||||||
| chr9:112714453 | A | C | 126 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(123): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.25+2008T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714453 | |||||||
| chr9:112714713 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0017g0137 |
2 | HG01175.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.25+1748T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714713 | |||||||
| chr9:112714901 | C | T | 6 | a0001c0001t0007g0045 a0001c0001t0007g0236 a0001c0001t0008g0022 others(3): Show |
8 | HG02109.hp2 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+1560G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112714901 | |||||||
| chr9:112715099 | T | C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+1362A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715099 | |||||||
| chr9:112715117 | CACATACA others(5): Show |
C | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+1332_25+1343del others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715117 | |||||||
| chr9:112715125 | TACATACA others(3): Show |
T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.25+1326_25+1335del others(10): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715125 | |||||||
| chr9:112715129 | T | C | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+1332A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715129 | |||||||
| chr9:112715133 | T | TAC | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(48): Show |
74 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.25+1326_25+1327dup others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | T | TACAC | 8 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
9 | HG01256.hp2 HG02300.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+1324_25+1327dup others(4): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | T | TACACAC | 3 | a0001c0001t0001g0044 a0001c0001t0028g0054 a0001c0001t0033g0271 |
4 | HG02280.hp2 HG02615.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1322_25+1327dup others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0232 a0001c0001t0035g0272 |
3 | HG03139.hp1 NA18950.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.25+1320_25+1327dup others(8): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.25+1316_25+1327dup others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TAC | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0023 others(37): Show |
49 | HG00609.hp1 HG00741.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.25+1326_25+1327del others(2): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACAC | T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
32 | HG00099.hp2 HG01175.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.25+1324_25+1327del others(4): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACACAC | T | 11 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0260 others(8): Show |
14 | HG00423.hp2 HG02145.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.25+1322_25+1327del others(6): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACACACA others(1): Show |
T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0046 others(49): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.25+1320_25+1327del others(8): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACACACA others(3): Show |
T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0087 a0001c0001t0001g0244 others(18): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.25+1318_25+1327del others(10): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.25+1316_25+1327del others(12): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715133 | TACACACA others(7): Show |
T | 7 | a0001c0001t0001g0092 a0001c0001t0005g0009 a0001c0001t0005g0050 others(4): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+1314_25+1327del others(14): Show |
INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715133 | |||||||
| chr9:112715139 | C | T | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+1322G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715139 | |||||||
| chr9:112715141 | C | T | 1 | a0001c0001t0025g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+1320G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715141 | |||||||
| chr9:112715242 | C | T | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+1219G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715242 | |||||||
| chr9:112715437 | T | A | 1 | a0001c0001t0034g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+1024A>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715437 | |||||||
| chr9:112715633 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0004g0259 |
2 | HG01993.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.25+828G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715633 | |||||||
| chr9:112715727 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG03017.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.25+734G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715727 | |||||||
| chr9:112715773 | CA | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
7 | HG00741.hp1 HG01361.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+687delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715773 | |||||||
| chr9:112715819 | T | G | 1 | a0001c0001t0003g0242 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.25+642A>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715819 | |||||||
| chr9:112715943 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG02572.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25+518A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112715943 | |||||||
| chr9:112716027 | A | G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+434T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112716027 | |||||||
| chr9:112716111 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.25+350G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112716111 | |||||||
| chr9:112716211 | T | C | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+250A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112716211 | |||||||
| chr9:112716260 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25+201G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 2/4 | chr9 | 112716260 | |||||||
| chr9:112716656 | A | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG02572.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-56-115T>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112716656 | |||||||
| chr9:112716682 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-56-141G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112716682 | |||||||
| chr9:112716762 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-56-221A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112716762 | |||||||
| chr9:112716763 | G | A | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-222C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112716763 | |||||||
| chr9:112716962 | C | CA | 15 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(12): Show |
17 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-56-422dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112716962 | |||||||
| chr9:112717144 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(16): Show |
31 | HG00621.hp1 HG02040.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.-56-603T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717144 | |||||||
| chr9:112717247 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-56-706A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717247 | |||||||
| chr9:112717307 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-57+680C>T | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717307 | |||||||
| chr9:112717328 | T | C | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+659A>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717328 | |||||||
| chr9:112717412 | G | C | 1 | a0001c0001t0020g0243 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-57+575C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717412 | |||||||
| chr9:112717515 | C | T | 1 | a0001c0001t0033g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-57+472G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717515 | |||||||
| chr9:112717527 | T | TA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00423.hp1 HG00621.hp2 HG01952.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57+459dupT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717527 | |||||||
| chr9:112717527 | TA | T | 11 | a0001c0001t0001g0066 a0001c0001t0002g0064 a0001c0001t0008g0022 others(8): Show |
12 | HG01168.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+459delT | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717527 | |||||||
| chr9:112717539 | A | C | 2 | a0001c0001t0034g0273 a0001c0001t0035g0272 |
2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-57+448T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717539 | |||||||
| chr9:112717612 | G | C | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+375C>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717612 | |||||||
| chr9:112717647 | A | G | 1 | a0001c0001t0013g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+340T>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717647 | |||||||
| chr9:112717692 | A | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0055 others(6): Show |
12 | HG01346.hp2 HG01433.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57+295T>G | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717692 | |||||||
| chr9:112717785 | C | T | 1 | a0001c0001t0028g0054 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-57+202G>A | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717785 | |||||||
| chr9:112717809 | T | G | 2 | a0001c0001t0034g0273 a0001c0001t0035g0272 |
2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-57+178A>C | INIP | ENSG00000148153.14 | transcript | ENST00000374242.9 | protein_coding | 1/4 | chr9 | 112717809 |