Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7461 |
|---|---|
| ensemblid | ENSG00000106665.16 |
| hgncid | 2586 |
| symbol | CLIP2 |
| name | CAP-Gly domain containing linker protein 2 |
| refseq_nuc | NM_003388.5 |
| refseq_prot | NP_003379.4 |
| ensembl_nuc | ENST00000223398.11 |
| ensembl_prot | ENSP00000223398.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 74289407 |
| end | 74405935 |
| strand | + |
| ver | v1.2 |
| region | chr7:74289407-74405935 |
| region5000 | chr7:74284407-74410935 |
| regionname0 | CLIP2_chr7_74289407_74405935 |
| regionname5000 | CLIP2_chr7_74284407_74410935 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1046 | 248 | 77 | 49 | 80 | 5 | 36 | 49 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002 | 0/0 | 1046 | 18 | 8 | 2 | 7 | 0 | 1 | 5 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003 | 1/0 | 1046 | 7 | 0 | 5 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0004 | 0/0 | 1046 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0005 | 0/0 | 1046 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0006 | 0/0 | 1046 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0007 | 0/0 | 1046 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0008 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3141 | 127 | 47 | 23 | 43 | 0 | 14 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0002 | 0/1 | 3141 | 99 | 22 | 22 | 31 | 5 | 18 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0003 | 0/0 | 3141 | 12 | 4 | 2 | 5 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0004 | 0/0 | 3141 | 7 | 0 | 0 | 5 | 0 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0005 | 1/0 | 3141 | 6 | 0 | 4 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0006 | 0/0 | 3141 | 5 | 4 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0007 | 0/0 | 3141 | 5 | 5 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0008 | 0/0 | 3141 | 3 | 2 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0009 | 0/0 | 3141 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0010 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0011 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0012 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0013 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0014 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0015 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0016 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0017 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0018 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0019 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0020 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| c0021 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2483 | 154 | 54 | 30 | 55 | 1 | 14 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0002 | 1/1 | 2483 | 64 | 10 | 16 | 26 | 3 | 7 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0003 | 0/0 | 2483 | 12 | 3 | 1 | 1 | 0 | 7 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0004 | 0/0 | 2483 | 9 | 0 | 3 | 3 | 0 | 3 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0005 | 0/0 | 2483 | 8 | 1 | 2 | 0 | 1 | 4 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0006 | 0/0 | 2483 | 5 | 3 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0007 | 0/0 | 2483 | 5 | 5 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0008 | 0/0 | 2481 | 4 | 4 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0009 | 0/0 | 2483 | 3 | 2 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0010 | 0/0 | 2483 | 3 | 3 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0011 | 0/0 | 2483 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0012 | 0/0 | 2483 | 2 | 0 | 0 | 0 | 0 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0013 | 0/0 | 2483 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0014 | 0/0 | 2483 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0015 | 0/0 | 2483 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0016 | 0/0 | 2483 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0017 | 0/0 | 2483 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0018 | 0/0 | 2483 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| t0019 | 0/0 | 2483 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3141 | 127 | 47 | 23 | 43 | 0 | 14 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002 | 0/1 | 3141 | 99 | 22 | 22 | 31 | 5 | 18 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0004 | 0/0 | 3141 | 7 | 0 | 0 | 5 | 0 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0007 | 0/0 | 3141 | 5 | 5 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0008 | 0/0 | 3141 | 3 | 2 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0009 | 0/0 | 3141 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0010 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0014 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0018 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0019 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0020 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0003 | 0/0 | 3141 | 12 | 4 | 2 | 5 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0006 | 0/0 | 3141 | 5 | 4 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0015 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003c0005 | 1/0 | 3141 | 6 | 0 | 4 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003c0011 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0004c0016 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0005c0012 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0006c0013 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0007c0017 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0008c0021 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5623 | 75 | 33 | 8 | 30 | 0 | 4 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0002 | 0/0 | 5623 | 25 | 2 | 10 | 10 | 0 | 3 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0003 | 0/0 | 5623 | 8 | 2 | 1 | 1 | 0 | 4 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0004 | 0/0 | 5623 | 4 | 0 | 1 | 1 | 0 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0005 | 0/0 | 5623 | 2 | 1 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0006 | 0/0 | 5623 | 4 | 3 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0007 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0008 | 0/0 | 5621 | 4 | 4 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0014 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0017 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0001t0019 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0001 | 0/0 | 5623 | 72 | 20 | 19 | 22 | 1 | 10 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0002 | 0/1 | 5623 | 15 | 1 | 2 | 7 | 2 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0003 | 0/0 | 5623 | 2 | 1 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0004 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0005 | 0/0 | 5623 | 6 | 0 | 1 | 0 | 1 | 4 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0015 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0016 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0002t0018 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0004t0001 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0004t0002 | 0/0 | 5623 | 4 | 0 | 0 | 4 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0004t0012 | 0/0 | 5623 | 2 | 0 | 0 | 0 | 0 | 2 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0007t0007 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0007t0010 | 0/0 | 5623 | 3 | 3 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0008t0009 | 0/0 | 5623 | 3 | 2 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0009t0001 | 0/0 | 5623 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0010t0003 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0014t0003 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0018t0001 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0019t0007 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0001c0020t0006 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0003t0002 | 0/0 | 5623 | 9 | 4 | 1 | 3 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0003t0004 | 0/0 | 5623 | 3 | 0 | 1 | 2 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0006t0002 | 0/0 | 5623 | 4 | 3 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0006t0013 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0002c0015t0002 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003c0005t0002 | 1/0 | 5623 | 4 | 0 | 2 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003c0005t0011 | 0/0 | 5623 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0003c0011t0002 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0004c0016t0001 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0005c0012t0001 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0006c0013t0002 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0007c0017t0004 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| a0008c0021t0001 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | copy fasta | chr7 | 74284407 | 74410935 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0014g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0017g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0001t0019g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0015g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0016g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0002t0018g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0012g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0004t0012g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0007t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0007t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0007t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0007t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0007t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0008t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0008t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0008t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0009t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0009t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0010t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0014t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0018t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0019t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0001c0020t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0006t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0006t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0006t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0006t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0002c0015t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0002g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0005t0011g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0003c0011t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0004c0016t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0005c0012t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0006c0013t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0007c0017t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| a0008c0021t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0249 | EUR | GBR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00099 | hp2 | a0001 | c0002 | t0015 | g0275 | EUR | GBR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0168 | EUR | GBR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00140 | hp2 | a0003 | c0005 | t0002 | g0176 | EUR | GBR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0121 | EUR | FIN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0257 | EUR | FIN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0198 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00438 | hp2 | a0002 | c0006 | t0002 | g0089 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00558 | hp1 | a0001 | c0004 | t0002 | g0175 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00639 | hp1 | a0001 | c0020 | t0006 | g0267 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00642 | hp2 | a0003 | c0005 | t0002 | g0179 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00673 | hp1 | a0001 | c0004 | t0002 | g0128 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0082 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01071 | hp1 | a0001 | c0009 | t0001 | g0126 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01099 | hp1 | a0003 | c0005 | t0011 | g0228 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01106 | hp2 | a0003 | c0005 | t0002 | g0173 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01175 | hp2 | a0003 | c0005 | t0011 | g0227 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01192 | hp1 | a0001 | c0008 | t0009 | g0211 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0049 | AMR | PUR | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01258 | hp2 | a0007 | c0017 | t0004 | g0075 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01928 | hp1 | a0005 | c0012 | t0001 | g0265 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01952 | hp2 | a0001 | c0001 | t0017 | g0260 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01975 | hp2 | a0002 | c0003 | t0004 | g0072 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01978 | hp2 | a0003 | c0011 | t0002 | g0242 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02015 | hp1 | a0002 | c0015 | t0002 | g0135 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02071 | hp2 | a0001 | c0004 | t0002 | g0132 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0278 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CDX | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | CDX | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02257 | hp2 | a0002 | c0006 | t0013 | g0042 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02280 | hp1 | a0001 | c0007 | t0007 | g0004 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02280 | hp2 | a0001 | c0007 | t0010 | g0015 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02451 | hp1 | a0001 | c0019 | t0007 | g0142 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02451 | hp2 | a0002 | c0006 | t0002 | g0023 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0166 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0177 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02717 | hp1 | a0001 | c0007 | t0007 | g0013 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0169 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02809 | hp1 | a0002 | c0003 | t0002 | g0203 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02886 | hp1 | a0004 | c0016 | t0001 | g0212 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0160 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03486 | hp1 | a0001 | c0008 | t0009 | g0149 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03490 | hp2 | a0001 | c0004 | t0012 | g0235 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03492 | hp1 | a0001 | c0004 | t0012 | g0236 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0116 | AFR | ESN | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03654 | hp2 | a0001 | c0002 | t0005 | g0240 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03669 | hp1 | a0001 | c0014 | t0003 | g0060 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0239 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0065 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0252 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04184 | hp2 | a0001 | c0001 | t0019 | g0067 | SAS | BEB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04199 | hp1 | a0001 | c0010 | t0003 | g0061 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04199 | hp2 | a0001 | c0002 | t0005 | g0127 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CHB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | CHB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18747 | hp2 | a0008 | c0021 | t0001 | g0136 | EAS | CHB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18906 | hp1 | a0002 | c0006 | t0002 | g0215 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0110 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18960 | hp2 | a0002 | c0003 | t0002 | g0183 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18979 | hp2 | a0001 | c0002 | t0016 | g0230 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18984 | hp1 | a0002 | c0003 | t0004 | g0054 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19002 | hp2 | a0001 | c0002 | t0018 | g0256 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | LWK | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0074 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19079 | hp2 | a0001 | c0018 | t0001 | g0095 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19082 | hp2 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | ASW | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA20129 | hp2 | a0001 | c0007 | t0010 | g0048 | AFR | ASW | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA20905 | hp1 | a0006 | c0013 | t0002 | g0084 | SAS | GIH | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0071 | SAS | GIH | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0079 | AMR | CLM | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02486 | hp1 | a0001 | c0007 | t0010 | g0010 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0147 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03471 | hp1 | a0001 | c0008 | t0009 | g0031 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | USA | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| HG06807 | hp2 | a0002 | c0006 | t0002 | g0040 | AFR | USA | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA21309 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | LWK | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0158 | REF | REF | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| homoSapiens_grch38 | hp1 | a0003 | c0005 | t0002 | g0258 | REF | REF | CLIP2_chr7_74284407_74410935 | CLIP2 | chr7 | 74284407 | 74410935 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74317586
|
G | T | 1 | a0008 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.40G>T | p.Gly14Trp | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/17 | 435/5623 | 40/3141 | 14/1046 | chr7 | 74317586 | ||
| chr7:74338861
|
C | T | 1 | a0007 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.535C>T | p.Pro179Ser | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 930/5623 | 535/3141 | 179/1046 | chr7 | 74338861 | ||
| chr7:74372953
|
G | A | 1 | a0006 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1402G>A | p.Ala468Thr | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/17 | 1797/5623 | 1402/3141 | 468/1046 | chr7 | 74372953 | ||
| chr7:74376628
|
C | T | 1 | a0005 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.2227C>T | p.Arg743Trp | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/17 | 2622/5623 | 2227/3141 | 743/1046 | chr7 | 74376628 | ||
| chr7:74376703
|
C | T | 1 | a0004 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.2302C>T | p.Arg768Trp | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/17 | 2697/5623 | 2302/3141 | 768/1046 | chr7 | 74376703 | ||
| chr7:74400372
|
C | A | 1 | a0002 | 18 | HG00438.hp2 HG01243.hp2 HG01975.hp2 others(15): Show |
missense_variant&splice_region_variant | MODERATE | c.2883C>A | p.Asp961Glu | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/17 | 3278/5623 | 2883/3141 | 961/1046 | chr7 | 74400372 | ||
| chr7:74400419
|
G | C | 7 | a0001a0002a0004others(4): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
missense_variant | MODERATE | c.2930G>C | p.Arg977Pro | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/17 | 3325/5623 | 2930/3141 | 977/1046 | chr7 | 74400419 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74317576
|
C | T | 1 | a0001c0004 | 7 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(4): Show |
synonymous_variant | LOW | c.30C>T | p.Pro10Pro | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/17 | 425/5623 | 30/3141 | 10/1046 | chr7 | 74317576 | ||
| chr7:74338482
|
C | T | 2 | a0001c0019a0001c0020 | 2 | HG00639.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.156C>T | p.Ser52Ser | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 551/5623 | 156/3141 | 52/1046 | chr7 | 74338482 | ||
| chr7:74338491
|
G | A | 1 | a0001c0010 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.165G>A | p.Pro55Pro | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 560/5623 | 165/3141 | 55/1046 | chr7 | 74338491 | ||
| chr7:74338692
|
C | T | 1 | a0001c0018 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.366C>T | p.Gly122Gly | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 761/5623 | 366/3141 | 122/1046 | chr7 | 74338692 | ||
| chr7:74338695
|
G | A | 2 | a0001c0019a0001c0020 | 2 | HG00639.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.369G>A | p.Ala123Ala | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 764/5623 | 369/3141 | 123/1046 | chr7 | 74338695 | ||
| chr7:74338803
|
C | T | 2 | a0001c0019a0001c0020 | 2 | HG00639.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.477C>T | p.His159His | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 872/5623 | 477/3141 | 159/1046 | chr7 | 74338803 | ||
| chr7:74338920
|
T | C | 8 | a0001c0002a0001c0009a0001c0018others(5): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
synonymous_variant | LOW | c.594T>C | p.Thr198Thr | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/17 | 989/5623 | 594/3141 | 198/1046 | chr7 | 74338920 | ||
| chr7:74353936
|
G | A | 1 | a0001c0009 | 2 | HG01070.hp2 HG01071.hp1 |
synonymous_variant | LOW | c.735G>A | p.Lys245Lys | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/17 | 1130/5623 | 735/3141 | 245/1046 | chr7 | 74353936 | ||
| chr7:74357450
|
T | C | 1 | a0001c0019 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1188T>C | p.Ile396Ile | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/17 | 1583/5623 | 1188/3141 | 396/1046 | chr7 | 74357450 | ||
| chr7:74376477
|
C | G | 1 | a0001c0008 | 3 | HG01192.hp1 HG03471.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.2076C>G | p.Ala692Ala | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/17 | 2471/5623 | 2076/3141 | 692/1046 | chr7 | 74376477 | ||
| chr7:74376618
|
C | T | 1 | a0004c0016 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2217C>T | p.Asp739Asp | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/17 | 2612/5623 | 2217/3141 | 739/1046 | chr7 | 74376618 | ||
| chr7:74389209
|
C | T | 1 | a0002c0015 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2670C>T | p.Asp890Asp | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/17 | 3065/5623 | 2670/3141 | 890/1046 | chr7 | 74389209 | ||
| chr7:74397149
|
T | C | 1 | a0001c0007 | 5 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
synonymous_variant | LOW | c.2796T>C | p.Arg932Arg | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/17 | 3191/5623 | 2796/3141 | 932/1046 | chr7 | 74397149 | ||
| chr7:74401531
|
C | T | 1 | a0001c0014 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.3093C>T | p.Asn1031Asn | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/17 | 3488/5623 | 3093/3141 | 1031/1046 | chr7 | 74401531 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74289609
|
C | T | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0019others(6): Show | 22 | HG00735.hp2 HG01258.hp2 HG01975.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-193C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/17 | 27938 | chr7 | 74289609 | |||||
| chr7:74404064
|
G | A | 1 | a0001c0008t0009 | 3 | HG01192.hp1 HG03471.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*216G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 216 | chr7 | 74404064 | |||||
| chr7:74404074
|
C | T | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(16): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*226C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 226 | chr7 | 74404074 | |||||
| chr7:74404108
|
G | A | 1 | a0001c0002t0015 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 260 | chr7 | 74404108 | |||||
| chr7:74404195
|
C | T | 2 | a0001c0001t0019a0001c0004t0012 | 3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*347C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 347 | chr7 | 74404195 | |||||
| chr7:74404248
|
G | A | 1 | a0001c0007t0010 | 3 | HG02280.hp2 HG02486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*400G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 400 | chr7 | 74404248 | |||||
| chr7:74404340
|
G | A | 2 | a0001c0001t0006a0001c0020t0006 | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 492 | chr7 | 74404340 | |||||
| chr7:74404557
|
C | T | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*709C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 709 | chr7 | 74404557 | |||||
| chr7:74404566
|
CAA | C | 1 | a0001c0001t0008 | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721delAA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 720 | INFO_REALIGN_3_PRIME | chr7 | 74404566 | ||||
| chr7:74404600
|
T | C | 1 | a0001c0002t0016 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 752 | chr7 | 74404600 | |||||
| chr7:74404601
|
C | T | 1 | a0001c0002t0016 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*753C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 753 | chr7 | 74404601 | |||||
| chr7:74404659
|
A | G | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*811A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 811 | chr7 | 74404659 | |||||
| chr7:74404747
|
T | C | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*899T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 899 | chr7 | 74404747 | |||||
| chr7:74404840
|
G | A | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*992G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 992 | chr7 | 74404840 | |||||
| chr7:74404861
|
C | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 182 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1013C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1013 | chr7 | 74404861 | |||||
| chr7:74405078
|
T | C | 1 | a0001c0001t0017 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1230T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1230 | chr7 | 74405078 | |||||
| chr7:74405333
|
T | C | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1485 | chr7 | 74405333 | |||||
| chr7:74405537
|
G | A | 1 | a0002c0006t0013 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1689G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1689 | chr7 | 74405537 | |||||
| chr7:74405569
|
G | A | 2 | a0001c0001t0006a0001c0020t0006 | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1721G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1721 | chr7 | 74405569 | |||||
| chr7:74405694
|
C | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(18): Show | 181 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1846C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 1846 | chr7 | 74405694 | |||||
| chr7:74405857
|
C | A | 4 | a0001c0001t0007a0001c0007t0007a0001c0007t0010others(1): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2009C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 2009 | chr7 | 74405857 | |||||
| chr7:74405910
|
C | T | 1 | a0001c0002t0018 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2062C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 17/17 | 2062 | chr7 | 74405910 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74289853
|
G | T | 1 | a0001c0001t0008g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-68+119G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74289853 | ||||||
| chr7:74289881
|
G | A | 1 | a0001c0004t0002g0001 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-68+147G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74289881 | ||||||
| chr7:74290335
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.-68+601T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74290335 | ||||||
| chr7:74290347
|
T | C | 225 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-68+613T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74290347 | ||||||
| chr7:74290507
|
G | C | 53 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-68+773G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74290507 | ||||||
| chr7:74290669
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-68+935G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74290669 | ||||||
| chr7:74290796
|
C | CTTCA | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+1067_-68+1070d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74290796 | |||||
| chr7:74291016
|
C | T | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0221others(3): Show | 6 | HG01433.hp1 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1282C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291016 | ||||||
| chr7:74291264
|
C | T | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | HG01081.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-68+1530C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291264 | ||||||
| chr7:74291390
|
C | T | 1 | a0001c0002t0015g0275 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-68+1656C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291390 | ||||||
| chr7:74291464
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-68+1730C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291464 | ||||||
| chr7:74291551
|
C | T | 54 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 54 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.-68+1817C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291551 | ||||||
| chr7:74291923
|
C | CT | 9 | a0001c0001t0001g0005a0001c0001t0001g0274a0001c0001t0002g0006others(6): Show | 9 | HG00558.hp2 HG01074.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+2207dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74291923 | |||||
| chr7:74291923
|
C | CTT | 70 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(67): Show | 70 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.-68+2206_-68+2207d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74291923 | |||||
| chr7:74291923
|
CT | C | 49 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(46): Show | 49 | HG00438.hp2 HG00733.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-68+2207delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74291923 | |||||
| chr7:74291987
|
C | T | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+2253C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291987 | ||||||
| chr7:74291995
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-68+2261G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74291995 | ||||||
| chr7:74292009
|
C | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+2275C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292009 | ||||||
| chr7:74292211
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+2477T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292211 | ||||||
| chr7:74292403
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+2669T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292403 | ||||||
| chr7:74292426
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-68+2692G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292426 | ||||||
| chr7:74292471
|
C | T | 2 | a0001c0002t0001g0216a0001c0002t0002g0119 | 2 | NA18940.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-68+2737C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292471 | ||||||
| chr7:74292514
|
A | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-68+2780A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292514 | ||||||
| chr7:74292527
|
C | G | 1 | a0007c0017t0004g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-68+2793C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292527 | ||||||
| chr7:74292868
|
C | G | 5 | a0001c0002t0001g0118a0001c0002t0001g0213a0001c0002t0001g0214others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+3134C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292868 | ||||||
| chr7:74292974
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-68+3240G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74292974 | ||||||
| chr7:74293140
|
C | T | 5 | a0001c0002t0001g0118a0001c0002t0001g0213a0001c0002t0001g0214others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+3406C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293140 | ||||||
| chr7:74293342
|
C | A | 1 | a0001c0002t0005g0079 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-68+3608C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293342 | ||||||
| chr7:74293414
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.-68+3680T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293414 | ||||||
| chr7:74293703
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-68+3969G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293703 | ||||||
| chr7:74293896
|
C | T | 76 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.-68+4162C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293896 | ||||||
| chr7:74293908
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-68+4174C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293908 | ||||||
| chr7:74293923
|
T | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 73 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.-68+4189T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74293923 | ||||||
| chr7:74294062
|
A | G | 1 | a0001c0008t0009g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-68+4328A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294062 | ||||||
| chr7:74294065
|
C | T | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-68+4331C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294065 | ||||||
| chr7:74294066
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-68+4332G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294066 | ||||||
| chr7:74294074
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-68+4340G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294074 | ||||||
| chr7:74294333
|
A | G | 78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-68+4599A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294333 | ||||||
| chr7:74294493
|
C | G | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-68+4759C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294493 | ||||||
| chr7:74294562
|
G | C | 1 | a0001c0001t0004g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-68+4828G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294562 | ||||||
| chr7:74294705
|
C | T | 1 | a0001c0008t0009g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-68+4971C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294705 | ||||||
| chr7:74294859
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-68+5125C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74294859 | ||||||
| chr7:74294918
|
G | GTAGTCTG others(7): Show |
1 | a0001c0001t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-68+5186_-68+5199d others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74294918 | |||||
| chr7:74295031
|
G | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-68+5297G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295031 | ||||||
| chr7:74295320
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-68+5586G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295320 | ||||||
| chr7:74295390
|
A | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-68+5656A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295390 | ||||||
| chr7:74295393
|
C | G | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0002c0003t0002g0116others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+5659C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295393 | ||||||
| chr7:74295485
|
G | A | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-68+5751G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295485 | ||||||
| chr7:74295628
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-68+5894G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295628 | ||||||
| chr7:74295644
|
A | C | 2 | a0001c0001t0001g0047a0001c0007t0010g0048 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-68+5910A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295644 | ||||||
| chr7:74295793
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+6059C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295793 | ||||||
| chr7:74295812
|
G | C | 78 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(75): Show | 78 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-68+6078G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295812 | ||||||
| chr7:74295822
|
G | T | 35 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0112others(32): Show | 35 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-68+6088G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295822 | ||||||
| chr7:74295883
|
G | GGATGCTG others(1): Show |
40 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-68+6151_-68+6158d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74295883 | |||||
| chr7:74295943
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0020others(57): Show | 60 | HG00558.hp2 HG00609.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.-68+6209C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74295943 | ||||||
| chr7:74295989
|
C | CA | 126 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0020others(123): Show | 126 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.-68+6275dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74295989 | |||||
| chr7:74295989
|
C | CAA | 19 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG00738.hp1 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-68+6274_-68+6275d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74295989 | |||||
| chr7:74295989
|
C | CAAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(4): Show | 7 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+6273_-68+6275d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74295989 | |||||
| chr7:74295989
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | HG02622.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+6266_-68+6275d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74295989 | |||||
| chr7:74296037
|
A | G | 1 | a0001c0002t0001g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-68+6303A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296037 | ||||||
| chr7:74296247
|
G | T | 5 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+6513G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296247 | ||||||
| chr7:74296571
|
T | C | 111 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0104others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-68+6837T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296571 | ||||||
| chr7:74296583
|
T | C | 108 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.-68+6849T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296583 | ||||||
| chr7:74296645
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-68+6911C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296645 | ||||||
| chr7:74296682
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-68+6948G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296682 | ||||||
| chr7:74296744
|
G | A | 1 | a0001c0010t0003g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-68+7010G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296744 | ||||||
| chr7:74296788
|
C | CAA | 91 | a0001c0001t0001g0104a0001c0001t0001g0162a0001c0001t0001g0171others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-68+7070_-68+7071d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74296788 | |||||
| chr7:74296788
|
C | CAAA | 8 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0002t0001g0094others(5): Show | 8 | HG00733.hp1 HG01168.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.-68+7069_-68+7071d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74296788 | |||||
| chr7:74296788
|
C | CAAAA | 6 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+7068_-68+7071d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74296788 | |||||
| chr7:74296788
|
CA | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0039others(4): Show | 7 | HG00639.hp1 HG01975.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+7071delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74296788 | |||||
| chr7:74296814
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-68+7080A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296814 | ||||||
| chr7:74296984
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+7250G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74296984 | ||||||
| chr7:74297230
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-68+7496T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297230 | ||||||
| chr7:74297485
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-68+7751A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297485 | ||||||
| chr7:74297497
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+7763G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297497 | ||||||
| chr7:74297563
|
C | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0114 | 2 | NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-68+7829C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297563 | ||||||
| chr7:74297789
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-68+8055G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297789 | ||||||
| chr7:74297790
|
G | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+8056G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297790 | ||||||
| chr7:74297802
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-68+8068G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297802 | ||||||
| chr7:74297871
|
C | T | 59 | a0001c0001t0001g0053a0001c0001t0001g0076a0001c0001t0001g0078others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-68+8137C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74297871 | ||||||
| chr7:74298143
|
G | A | 5 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+8409G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298143 | ||||||
| chr7:74298161
|
A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 96 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.-68+8427A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298161 | ||||||
| chr7:74298356
|
G | GT | 36 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0092others(33): Show | 36 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-68+8641dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74298356 | |||||
| chr7:74298356
|
G | T | 3 | a0001c0001t0001g0047a0001c0002t0018g0256a0001c0020t0006g0267 | 3 | HG00639.hp1 HG01081.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-68+8622G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298356 | ||||||
| chr7:74298356
|
GT | G | 81 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0154others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.-68+8641delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74298356 | |||||
| chr7:74298358
|
T | G | 1 | a0001c0018t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-68+8624T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298358 | ||||||
| chr7:74298363
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-68+8629T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298363 | ||||||
| chr7:74298570
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-68+8836C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298570 | ||||||
| chr7:74298583
|
AGTGGC | A | 181 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-68+8858_-68+8862d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74298583 | |||||
| chr7:74298706
|
G | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+8972G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298706 | ||||||
| chr7:74298791
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+9057G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74298791 | ||||||
| chr7:74299023
|
C | T | 1 | a0007c0017t0004g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-68+9289C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299023 | ||||||
| chr7:74299279
|
T | C | 212 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-68+9545T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299279 | ||||||
| chr7:74299324
|
A | AAAAT | 20 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(17): Show | 20 | HG01081.hp2 HG01099.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-68+9630_-68+9633d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299324 | |||||
| chr7:74299324
|
A | AAAATAAA others(5): Show |
1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+9622_-68+9633d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299324 | |||||
| chr7:74299324
|
AAAAT | A | 39 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0076others(36): Show | 39 | HG01074.hp2 HG01099.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.-68+9630_-68+9633d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299324 | |||||
| chr7:74299324
|
AAAATAAA others(1): Show |
A | 40 | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0086others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-68+9626_-68+9633d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299324 | |||||
| chr7:74299324
|
AAAATAAA others(5): Show |
A | 107 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-68+9622_-68+9633d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299324 | |||||
| chr7:74299366
|
A | AATAAATA others(9): Show |
1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-68+9633_-68+9634i others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299366 | |||||
| chr7:74299548
|
T | C | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+9814T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299548 | ||||||
| chr7:74299560
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-68+9826C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299560 | ||||||
| chr7:74299584
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-68+9850C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299584 | ||||||
| chr7:74299704
|
C | T | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+9970C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299704 | ||||||
| chr7:74299775
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10041C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299775 | ||||||
| chr7:74299776
|
G | T | 9 | a0001c0002t0001g0251a0001c0002t0001g0276a0001c0002t0001g0277others(6): Show | 9 | HG00323.hp2 HG01081.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+10042G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299776 | ||||||
| chr7:74299791
|
C | T | 1 | a0001c0002t0005g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-68+10057C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299791 | ||||||
| chr7:74299843
|
A | AT | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+10110dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74299843 | |||||
| chr7:74299871
|
A | G | 1 | a0001c0002t0001g0186 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-68+10137A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299871 | ||||||
| chr7:74299925
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-68+10191G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74299925 | ||||||
| chr7:74300070
|
T | A | 5 | a0001c0002t0001g0007a0001c0002t0001g0041a0002c0006t0002g0023others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+10336T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300070 | ||||||
| chr7:74300181
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10447T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300181 | ||||||
| chr7:74300232
|
C | T | 38 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(35): Show | 38 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-68+10498C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300232 | ||||||
| chr7:74300253
|
C | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10519C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300253 | ||||||
| chr7:74300274
|
C | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10540C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300274 | ||||||
| chr7:74300406
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10672T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300406 | ||||||
| chr7:74300453
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-68+10719C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300453 | ||||||
| chr7:74300457
|
CT | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-68+10739delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74300457 | |||||
| chr7:74300478
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-68+10744C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300478 | ||||||
| chr7:74300612
|
C | T | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-68+10878C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300612 | ||||||
| chr7:74300613
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+10879G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300613 | ||||||
| chr7:74300807
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-68+11073G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300807 | ||||||
| chr7:74300945
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+11211C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74300945 | ||||||
| chr7:74301087
|
A | C | 1 | a0002c0003t0002g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-68+11353A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301087 | ||||||
| chr7:74301374
|
C | CTTA | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+11652_-68+1165 others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74301374 | |||||
| chr7:74301428
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-68+11694G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301428 | ||||||
| chr7:74301508
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+11774G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301508 | ||||||
| chr7:74301539
|
T | C | 111 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-68+11805T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301539 | ||||||
| chr7:74301543
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-68+11809C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301543 | ||||||
| chr7:74301549
|
A | ATT | 109 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.-68+11828_-68+1182 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74301549 | |||||
| chr7:74301580
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-68+11846C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301580 | ||||||
| chr7:74301638
|
C | A | 1 | a0001c0002t0003g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-68+11904C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301638 | ||||||
| chr7:74301714
|
G | GT | 109 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.-68+11988dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74301714 | |||||
| chr7:74301768
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0114 | 2 | NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-68+12034G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301768 | ||||||
| chr7:74301772
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+12038G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301772 | ||||||
| chr7:74301960
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+12226G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74301960 | ||||||
| chr7:74302279
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+12545G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302279 | ||||||
| chr7:74302342
|
A | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+12608A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302342 | ||||||
| chr7:74302361
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-68+12627G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302361 | ||||||
| chr7:74302448
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-68+12714C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302448 | ||||||
| chr7:74302841
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-68+13107G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302841 | ||||||
| chr7:74302899
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-68+13165C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302899 | ||||||
| chr7:74302901
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-68+13167G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302901 | ||||||
| chr7:74302976
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-68+13242G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74302976 | ||||||
| chr7:74303136
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-68+13402G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303136 | ||||||
| chr7:74303201
|
G | A | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-68+13467G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303201 | ||||||
| chr7:74303594
|
A | AT | 73 | a0001c0001t0001g0027a0001c0001t0001g0076a0001c0001t0001g0085others(70): Show | 73 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-67-13866dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74303594 | |||||
| chr7:74303594
|
AT | A | 18 | a0001c0001t0001g0120a0001c0002t0001g0105a0001c0002t0001g0121others(15): Show | 18 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67-13866delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74303594 | |||||
| chr7:74303607
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-68+13873T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303607 | ||||||
| chr7:74303649
|
C | T | 5 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(2): Show | 5 | HG01243.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-13831C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303649 | ||||||
| chr7:74303828
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-67-13652C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303828 | ||||||
| chr7:74303874
|
T | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0172 | 2 | HG01168.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-67-13606T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303874 | ||||||
| chr7:74303879
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-13601T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74303879 | ||||||
| chr7:74303911
|
C | CA | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-67-13552dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74303911 | |||||
| chr7:74303911
|
C | CAA | 105 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.-67-13553_-67-1355 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74303911 | |||||
| chr7:74304008
|
G | A | 6 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(3): Show | 6 | HG00639.hp1 HG01243.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-13472G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304008 | ||||||
| chr7:74304065
|
C | T | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-67-13415C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304065 | ||||||
| chr7:74304080
|
A | AT | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67-13388dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74304080 | |||||
| chr7:74304080
|
A | ATT | 81 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0053others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-67-13389_-67-1338 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74304080 | |||||
| chr7:74304149
|
A | G | 1 | a0001c0002t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-67-13331A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304149 | ||||||
| chr7:74304201
|
G | A | 1 | a0001c0002t0005g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-67-13279G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304201 | ||||||
| chr7:74304313
|
G | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-67-13167G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304313 | ||||||
| chr7:74304467
|
A | G | 2 | a0001c0002t0001g0190a0001c0002t0001g0199 | 2 | HG00408.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-67-13013A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304467 | ||||||
| chr7:74304489
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-67-12991G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304489 | ||||||
| chr7:74304556
|
C | CA | 105 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0104others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-67-12910dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74304556 | |||||
| chr7:74304679
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-67-12801C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304679 | ||||||
| chr7:74304802
|
G | A | 6 | a0001c0001t0001g0120a0001c0002t0001g0204a0001c0002t0001g0217others(3): Show | 6 | HG00639.hp1 HG01243.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-12678G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304802 | ||||||
| chr7:74304956
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0002g0001 | 2 | HG02074.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-67-12524A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304956 | ||||||
| chr7:74304968
|
G | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-67-12512G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74304968 | ||||||
| chr7:74304968
|
G | GAATA | 8 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0113others(5): Show | 8 | HG00639.hp1 HG01258.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-12493_-67-1249 others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74304968 | |||||
| chr7:74305031
|
C | T | 1 | a0003c0005t0002g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-67-12449C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305031 | ||||||
| chr7:74305066
|
G | A | 94 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(91): Show | 94 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-67-12414G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305066 | ||||||
| chr7:74305143
|
T | C | 116 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0120others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.-67-12337T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305143 | ||||||
| chr7:74305152
|
T | TGTCCAGC others(14): Show |
108 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.-67-12327_-67-1230 others(25): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74305152 | |||||
| chr7:74305207
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-67-12273C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305207 | ||||||
| chr7:74305231
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-67-12249C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305231 | ||||||
| chr7:74305375
|
G | A | 33 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0037others(30): Show | 33 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-67-12105G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305375 | ||||||
| chr7:74305528
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-67-11952T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305528 | ||||||
| chr7:74305550
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-67-11930A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305550 | ||||||
| chr7:74305601
|
C | G | 1 | a0001c0001t0008g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-67-11879C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305601 | ||||||
| chr7:74305635
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-67-11845A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305635 | ||||||
| chr7:74305650
|
C | T | 7 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(4): Show | 7 | HG00621.hp2 HG02056.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-11830C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305650 | ||||||
| chr7:74305855
|
A | AC | 55 | a0001c0001t0001g0043a0001c0001t0001g0112a0001c0001t0001g0153others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-67-11616dupC | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74305855 | |||||
| chr7:74305855
|
A | ACC | 22 | a0001c0001t0001g0019a0001c0001t0001g0078a0001c0001t0001g0114others(19): Show | 22 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-67-11617_-67-1161 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74305855 | |||||
| chr7:74305859
|
C | G | 2 | a0001c0002t0001g0141a0001c0002t0001g0167 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-67-11621C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305859 | ||||||
| chr7:74305864
|
CA | C | 49 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(46): Show | 49 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-67-11615delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305864 | ||||||
| chr7:74305865
|
A | C | 177 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0027others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-67-11615A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305865 | ||||||
| chr7:74305868
|
G | C | 61 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(58): Show | 61 | HG00558.hp2 HG00735.hp2 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.-67-11612G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305868 | ||||||
| chr7:74305873
|
T | C | 61 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(58): Show | 61 | HG00558.hp2 HG00735.hp2 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.-67-11607T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74305873 | ||||||
| chr7:74306043
|
T | C | 6 | a0001c0001t0001g0047a0001c0002t0001g0204a0001c0002t0001g0217others(3): Show | 6 | HG01081.hp2 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-11437T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306043 | ||||||
| chr7:74306048
|
C | A | 2 | a0001c0001t0001g0047a0001c0019t0007g0142 | 2 | HG01081.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-67-11432C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306048 | ||||||
| chr7:74306230
|
C | T | 2 | a0001c0002t0001g0237a0001c0002t0002g0238 | 2 | NA18951.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-67-11250C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306230 | ||||||
| chr7:74306400
|
C | A | 1 | a0001c0002t0001g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-67-11080C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306400 | ||||||
| chr7:74306417
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-67-11063C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306417 | ||||||
| chr7:74306431
|
G | A | 11 | a0001c0001t0001g0233a0001c0002t0001g0170a0001c0002t0001g0190others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-11049G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306431 | ||||||
| chr7:74306651
|
C | T | 96 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(93): Show | 96 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.-67-10829C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306651 | ||||||
| chr7:74306679
|
A | C | 114 | a0001c0001t0001g0047a0001c0001t0001g0087a0001c0001t0001g0104others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-67-10801A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306679 | ||||||
| chr7:74306769
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-67-10711C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306769 | ||||||
| chr7:74306770
|
G | A | 2 | a0001c0002t0001g0237a0001c0002t0002g0238 | 2 | NA18951.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-67-10710G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74306770 | ||||||
| chr7:74307079
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0159a0001c0002t0001g0163others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-10401C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307079 | ||||||
| chr7:74307274
|
T | C | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-67-10206T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307274 | ||||||
| chr7:74307326
|
C | T | 2 | a0001c0001t0005g0018a0001c0001t0005g0206 | 2 | HG00738.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-67-10154C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307326 | ||||||
| chr7:74307406
|
G | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG00621.hp1 NA18945.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-10074G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307406 | ||||||
| chr7:74307465
|
T | C | 1 | a0005c0012t0001g0265 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-67-10015T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307465 | ||||||
| chr7:74307796
|
AGGTTCTT others(23): Show |
A | 1 | a0001c0001t0001g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-67-9678_-67-9649d others(32): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74307796 | |||||
| chr7:74307826
|
T | G | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-9654T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307826 | ||||||
| chr7:74307921
|
G | A | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-9559G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74307921 | ||||||
| chr7:74308117
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-67-9363G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308117 | ||||||
| chr7:74308247
|
G | A | 36 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0037others(33): Show | 36 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-67-9233G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308247 | ||||||
| chr7:74308275
|
C | T | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-9205C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308275 | ||||||
| chr7:74308342
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-67-9138C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308342 | ||||||
| chr7:74308412
|
A | G | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-67-9068A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308412 | ||||||
| chr7:74308489
|
C | T | 1 | a0001c0001t0008g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-67-8991C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308489 | ||||||
| chr7:74308837
|
G | A | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-8643G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74308837 | ||||||
| chr7:74309086
|
C | T | 2 | a0001c0002t0004g0071a0001c0002t0005g0166 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-67-8394C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309086 | ||||||
| chr7:74309243
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-8237A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309243 | ||||||
| chr7:74309280
|
A | G | 1 | a0002c0003t0002g0110 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-67-8200A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309280 | ||||||
| chr7:74309294
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-67-8186G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309294 | ||||||
| chr7:74309333
|
T | G | 1 | a0001c0002t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-67-8147T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309333 | ||||||
| chr7:74309410
|
A | C | 1 | a0001c0002t0001g0254 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-67-8070A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309410 | ||||||
| chr7:74309483
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-7997C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309483 | ||||||
| chr7:74309592
|
A | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0019others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-67-7888A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309592 | ||||||
| chr7:74309634
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-67-7846G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309634 | ||||||
| chr7:74309658
|
A | G | 113 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.-67-7822A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309658 | ||||||
| chr7:74309689
|
C | T | 5 | a0001c0004t0001g0107a0001c0004t0002g0001a0001c0004t0002g0128others(2): Show | 5 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-7791C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309689 | ||||||
| chr7:74309826
|
CA | C | 114 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-67-7639delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74309826 | |||||
| chr7:74309934
|
C | T | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-67-7546C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74309934 | ||||||
| chr7:74310036
|
C | CA | 40 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0052others(37): Show | 40 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-67-7402dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAA | 15 | a0001c0001t0001g0027a0001c0001t0001g0137a0001c0001t0001g0148others(12): Show | 15 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67-7403_-67-7402d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAA | 12 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0143others(9): Show | 12 | HG00673.hp1 HG01243.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.-67-7406_-67-7402d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAAA | 9 | a0001c0001t0001g0208a0001c0001t0001g0219a0001c0001t0001g0220others(6): Show | 9 | HG01099.hp2 HG01123.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-67-7407_-67-7402d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0262 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-67-7411_-67-7402d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-67-7413_-67-7402d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-67-7414_-67-7402d others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02622.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-67-7415_-67-7402d others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CA | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG02630.hp2 HG02818.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-7402delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0145a0001c0001t0002g0006a0001c0001t0014g0198 | 3 | HG00408.hp2 HG00558.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-67-7411_-67-7402d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0002g0077others(3): Show | 6 | HG02083.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-7412_-67-7402d others(13): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0076a0001c0001t0001g0202a0001c0001t0006g0002others(4): Show | 7 | HG01074.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-7413_-67-7402d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0002g0046a0001c0001t0002g0051a0001c0001t0008g0029others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67-7414_-67-7402d others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0178a0001c0001t0001g0180a0002c0003t0002g0177 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-67-7415_-67-7402d others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-7416_-67-7402d others(17): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0002t0001g0131a0001c0007t0007g0013 | 2 | HG01433.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-67-7419_-67-7402d others(20): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(18): Show |
C | 2 | a0001c0002t0001g0210a0001c0002t0001g0216 | 2 | HG00741.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-67-7426_-67-7402d others(27): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310036
|
CAAAAAAA others(19): Show |
C | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-67-7427_-67-7402d others(28): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310036 | |||||
| chr7:74310309
|
C | G | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-7171C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310309 | ||||||
| chr7:74310426
|
G | A | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-67-7054G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310426 | ||||||
| chr7:74310580
|
C | T | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-6900C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310580 | ||||||
| chr7:74310632
|
C | T | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-6848C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310632 | ||||||
| chr7:74310776
|
A | G | 11 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(8): Show | 11 | HG01433.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-67-6704A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310776 | ||||||
| chr7:74310814
|
C | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-6666C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310814 | ||||||
| chr7:74310881
|
G | C | 1 | a0001c0002t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-67-6599G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74310881 | ||||||
| chr7:74310983
|
C | CT | 111 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-67-6483dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74310983 | |||||
| chr7:74311080
|
C | T | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-67-6400C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311080 | ||||||
| chr7:74311104
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-6376C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311104 | ||||||
| chr7:74311200
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-67-6280C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311200 | ||||||
| chr7:74311470
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-67-6010G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311470 | ||||||
| chr7:74311530
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-5950C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311530 | ||||||
| chr7:74311622
|
A | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-5858A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311622 | ||||||
| chr7:74311864
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-67-5616A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311864 | ||||||
| chr7:74311876
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-67-5604C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311876 | ||||||
| chr7:74311892
|
A | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-5588A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311892 | ||||||
| chr7:74311907
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-67-5573A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311907 | ||||||
| chr7:74311918
|
A | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-67-5562A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311918 | ||||||
| chr7:74311932
|
AG | A | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-67-5547delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311932 | ||||||
| chr7:74311933
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-67-5547G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311933 | ||||||
| chr7:74311944
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-67-5536A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74311944 | ||||||
| chr7:74312116
|
T | G | 1 | a0001c0001t0002g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-67-5364T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312116 | ||||||
| chr7:74312233
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-67-5247G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312233 | ||||||
| chr7:74312258
|
A | T | 2 | a0001c0002t0001g0159a0001c0002t0001g0164 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-67-5222A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312258 | ||||||
| chr7:74312259
|
T | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0019others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-67-5221T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312259 | ||||||
| chr7:74312552
|
C | G | 1 | a0001c0002t0001g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-67-4928C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312552 | ||||||
| chr7:74312597
|
C | T | 1 | a0001c0002t0002g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-67-4883C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312597 | ||||||
| chr7:74312641
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-4839G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312641 | ||||||
| chr7:74312643
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-67-4837C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312643 | ||||||
| chr7:74312665
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0195 | 2 | HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-67-4815C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312665 | ||||||
| chr7:74312718
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-67-4762A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312718 | ||||||
| chr7:74312868
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-67-4612A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312868 | ||||||
| chr7:74312913
|
C | T | 52 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.-67-4567C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312913 | ||||||
| chr7:74312919
|
A | G | 51 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-67-4561A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74312919 | ||||||
| chr7:74313131
|
C | T | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-67-4349C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313131 | ||||||
| chr7:74313326
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-4154G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313326 | ||||||
| chr7:74313375
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-4105T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313375 | ||||||
| chr7:74313377
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-4103G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313377 | ||||||
| chr7:74313452
|
C | T | 1 | a0001c0002t0002g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-67-4028C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313452 | ||||||
| chr7:74313483
|
C | G | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-67-3997C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313483 | ||||||
| chr7:74313552
|
TC | T | 4 | a0001c0002t0001g0081a0001c0002t0001g0090a0001c0002t0001g0096others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67-3926delC | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74313552 | |||||
| chr7:74313625
|
C | G | 114 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-67-3855C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313625 | ||||||
| chr7:74313703
|
C | CA | 112 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-67-3776dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74313703 | |||||
| chr7:74313779
|
T | C | 113 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.-67-3701T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74313779 | ||||||
| chr7:74314179
|
C | CAAA | 107 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-67-3286_-67-3284d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74314179 | |||||
| chr7:74314219
|
G | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(4): Show | 7 | HG01099.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-3261G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74314219 | ||||||
| chr7:74314245
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-3235T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74314245 | ||||||
| chr7:74314345
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-67-3135G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74314345 | ||||||
| chr7:74314593
|
T | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-2887T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74314593 | ||||||
| chr7:74314948
|
G | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG02630.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-2532G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74314948 | ||||||
| chr7:74315002
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-67-2478C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74315002 | ||||||
| chr7:74315027
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-67-2453A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74315027 | ||||||
| chr7:74315248
|
C | G | 2 | a0001c0002t0001g0102a0001c0002t0001g0229 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-67-2232C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74315248 | ||||||
| chr7:74315262
|
C | A | 1 | a0001c0001t0005g0206 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-67-2218C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74315262 | ||||||
| chr7:74315351
|
C | CT | 79 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0053others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.-67-2118dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74315351 | |||||
| chr7:74315889
|
A | T | 101 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0153others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.-67-1591A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74315889 | ||||||
| chr7:74316009
|
C | T | 2 | a0001c0002t0001g0118a0001c0002t0001g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-67-1471C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74316009 | ||||||
| chr7:74316452
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-67-1028C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74316452 | ||||||
| chr7:74316560
|
C | CT | 7 | a0001c0001t0001g0037a0001c0001t0004g0066a0001c0002t0001g0115others(4): Show | 7 | HG00642.hp2 HG01978.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-907dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 74316560 | |||||
| chr7:74316734
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-67-746G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74316734 | ||||||
| chr7:74316826
|
T | C | 2 | a0001c0001t0001g0233a0001c0002t0001g0234 | 2 | HG00438.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-67-654T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74316826 | ||||||
| chr7:74317249
|
G | T | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-67-231G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74317249 | ||||||
| chr7:74317280
|
T | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67-200T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74317280 | ||||||
| chr7:74317339
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-67-141C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 1/16 | chr7 | 74317339 | ||||||
| chr7:74317712
|
G | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0053others(64): Show | 67 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.121+45G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74317712 | ||||||
| chr7:74317859
|
G | A | 1 | a0002c0003t0002g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.121+192G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74317859 | ||||||
| chr7:74317860
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121+193C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74317860 | ||||||
| chr7:74317929
|
C | T | 1 | a0002c0003t0002g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.121+262C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74317929 | ||||||
| chr7:74318112
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+445C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318112 | ||||||
| chr7:74318188
|
A | G | 1 | a0001c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.121+521A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318188 | ||||||
| chr7:74318221
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+554G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318221 | ||||||
| chr7:74318253
|
G | T | 125 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0138others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.121+586G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318253 | ||||||
| chr7:74318533
|
G | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+866G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318533 | ||||||
| chr7:74318569
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+902C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318569 | ||||||
| chr7:74318598
|
A | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.121+931A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318598 | ||||||
| chr7:74318701
|
G | T | 1 | a0001c0002t0001g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.121+1034G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318701 | ||||||
| chr7:74318759
|
T | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0254 | 2 | HG00735.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.121+1092T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318759 | ||||||
| chr7:74318877
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121+1210G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318877 | ||||||
| chr7:74318892
|
C | T | 4 | a0001c0002t0001g0118a0001c0002t0001g0131a0001c0002t0001g0213others(1): Show | 4 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+1225C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74318892 | ||||||
| chr7:74319236
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.121+1569G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319236 | ||||||
| chr7:74319368
|
G | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+1701G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319368 | ||||||
| chr7:74319408
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+1741C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319408 | ||||||
| chr7:74319460
|
C | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+1793C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319460 | ||||||
| chr7:74319606
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+1939C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319606 | ||||||
| chr7:74319622
|
A | G | 1 | a0001c0002t0001g0165 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.121+1955A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74319622 | ||||||
| chr7:74319824
|
AAG | A | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+2167_121+2168d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74319824 | |||||
| chr7:74320195
|
CA | C | 126 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0104others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.121+2549delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74320195 | |||||
| chr7:74320200
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121+2533A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320200 | ||||||
| chr7:74320212
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+2545A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320212 | ||||||
| chr7:74320213
|
A | G | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+2546A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320213 | ||||||
| chr7:74320222
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.121+2555A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320222 | ||||||
| chr7:74320354
|
C | T | 1 | a0001c0001t0008g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+2687C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320354 | ||||||
| chr7:74320389
|
G | A | 40 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(37): Show | 40 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.121+2722G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320389 | ||||||
| chr7:74320508
|
C | T | 2 | a0001c0002t0001g0088a0001c0002t0002g0098 | 2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.121+2841C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320508 | ||||||
| chr7:74320828
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+3161G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74320828 | ||||||
| chr7:74320955
|
CGA | C | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+3294_121+3295d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74320955 | |||||
| chr7:74321005
|
G | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0037others(32): Show | 35 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.121+3338G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321005 | ||||||
| chr7:74321005
|
G | C | 2 | a0001c0002t0001g0226a0001c0002t0002g0273 | 2 | HG00621.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.121+3338G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321005 | ||||||
| chr7:74321142
|
A | C | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.121+3475A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321142 | ||||||
| chr7:74321265
|
C | T | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+3598C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321265 | ||||||
| chr7:74321479
|
A | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0143 | 2 | HG01258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121+3812A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321479 | ||||||
| chr7:74321533
|
G | A | 2 | a0001c0002t0001g0204a0001c0002t0001g0217 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.121+3866G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321533 | ||||||
| chr7:74321609
|
C | T | 1 | a0001c0007t0010g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.121+3942C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321609 | ||||||
| chr7:74321617
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+3950C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321617 | ||||||
| chr7:74321714
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+4047C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321714 | ||||||
| chr7:74321888
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+4221C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74321888 | ||||||
| chr7:74321986
|
C | CT | 120 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.121+4334dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74321986 | |||||
| chr7:74322271
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+4604G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322271 | ||||||
| chr7:74322351
|
A | G | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.121+4684A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322351 | ||||||
| chr7:74322374
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+4707G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322374 | ||||||
| chr7:74322688
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+5021G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322688 | ||||||
| chr7:74322723
|
T | G | 2 | a0001c0001t0002g0188a0001c0001t0003g0063 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.121+5056T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322723 | ||||||
| chr7:74322761
|
T | C | 2 | a0001c0001t0001g0224a0001c0008t0009g0031 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.121+5094T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322761 | ||||||
| chr7:74322833
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.121+5166C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322833 | ||||||
| chr7:74322887
|
T | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+5220T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74322887 | ||||||
| chr7:74323081
|
T | TTTTA | 10 | a0001c0001t0001g0052a0001c0001t0001g0114a0001c0001t0002g0046others(7): Show | 10 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+5458_121+5461d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323081
|
T | TTTTATTT others(1): Show |
3 | a0001c0001t0001g0078a0002c0003t0002g0183a0002c0003t0004g0054 | 3 | NA18960.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.121+5454_121+5461d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323081
|
TTTTA | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(30): Show | 33 | HG00558.hp2 HG00733.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.121+5458_121+5461d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323081
|
TTTTATTT others(1): Show |
T | 112 | a0001c0001t0001g0045a0001c0001t0001g0104a0001c0001t0001g0153others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.121+5454_121+5461d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323081
|
TTTTATTT others(5): Show |
T | 4 | a0001c0001t0001g0085a0001c0001t0001g0144a0001c0001t0001g0172others(1): Show | 4 | HG01168.hp1 HG02738.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+5450_121+5461d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323081
|
TTTTATTT others(9): Show |
T | 70 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0053others(67): Show | 70 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.121+5446_121+5461d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74323081 | |||||
| chr7:74323126
|
T | C | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(4): Show | 7 | HG01099.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+5459T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323126 | ||||||
| chr7:74323145
|
C | G | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+5478C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323145 | ||||||
| chr7:74323379
|
G | A | 11 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(8): Show | 11 | HG01433.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.121+5712G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323379 | ||||||
| chr7:74323402
|
A | G | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.121+5735A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323402 | ||||||
| chr7:74323631
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.121+5964T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323631 | ||||||
| chr7:74323650
|
C | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+5983C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323650 | ||||||
| chr7:74323737
|
G | A | 201 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0019others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.121+6070G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323737 | ||||||
| chr7:74323765
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+6098C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323765 | ||||||
| chr7:74323769
|
C | T | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.121+6102C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323769 | ||||||
| chr7:74323931
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+6264G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74323931 | ||||||
| chr7:74324030
|
C | T | 1 | a0002c0003t0002g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.121+6363C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324030 | ||||||
| chr7:74324234
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.121+6567C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324234 | ||||||
| chr7:74324259
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121+6592C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324259 | ||||||
| chr7:74324267
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121+6600C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324267 | ||||||
| chr7:74324336
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+6669A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324336 | ||||||
| chr7:74324375
|
T | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+6708T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324375 | ||||||
| chr7:74324572
|
A | G | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+6905A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324572 | ||||||
| chr7:74324683
|
C | T | 3 | a0001c0001t0003g0064a0001c0001t0004g0066a0001c0002t0003g0065 | 3 | HG00735.hp2 HG01978.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.121+7016C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324683 | ||||||
| chr7:74324818
|
G | GA | 9 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0076others(6): Show | 9 | HG00621.hp1 HG01081.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+7171dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74324818 | |||||
| chr7:74324818
|
GA | G | 118 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.121+7171delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74324818 | |||||
| chr7:74324821
|
A | G | 1 | a0002c0003t0002g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.121+7154A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324821 | ||||||
| chr7:74324902
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.121+7235C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74324902 | ||||||
| chr7:74325059
|
C | T | 3 | a0001c0002t0001g0186a0001c0002t0001g0225a0001c0002t0002g0158 | 3 | HG00733.hp2 HG01168.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.121+7392C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325059 | ||||||
| chr7:74325110
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.121+7443C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325110 | ||||||
| chr7:74325136
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+7469A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325136 | ||||||
| chr7:74325259
|
G | A | 124 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.121+7592G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325259 | ||||||
| chr7:74325309
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.121+7642C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325309 | ||||||
| chr7:74325535
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+7868T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325535 | ||||||
| chr7:74325549
|
G | A | 1 | a0001c0002t0002g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.121+7882G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325549 | ||||||
| chr7:74325600
|
C | T | 2 | a0001c0009t0001g0082a0001c0009t0001g0126 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.121+7933C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325600 | ||||||
| chr7:74325668
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.121+8001C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325668 | ||||||
| chr7:74325764
|
T | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.121+8097T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325764 | ||||||
| chr7:74325801
|
C | T | 40 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(37): Show | 40 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.121+8134C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325801 | ||||||
| chr7:74325896
|
G | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+8229G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325896 | ||||||
| chr7:74325921
|
A | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.121+8254A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74325921 | ||||||
| chr7:74326068
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121+8401G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326068 | ||||||
| chr7:74326109
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+8442A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326109 | ||||||
| chr7:74326263
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+8596G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326263 | ||||||
| chr7:74326284
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.121+8617G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326284 | ||||||
| chr7:74326377
|
G | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0053others(65): Show | 68 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.121+8710G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326377 | ||||||
| chr7:74326384
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+8717C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326384 | ||||||
| chr7:74326397
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.121+8730G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326397 | ||||||
| chr7:74326638
|
A | AT | 6 | a0001c0001t0002g0259a0001c0001t0005g0206a0001c0002t0001g0197others(3): Show | 6 | HG01192.hp2 HG02055.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+8987dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74326638 | |||||
| chr7:74326680
|
C | T | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.121+9013C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326680 | ||||||
| chr7:74326785
|
T | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+9118T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326785 | ||||||
| chr7:74326826
|
C | T | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.121+9159C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326826 | ||||||
| chr7:74326943
|
G | T | 1 | a0001c0002t0001g0197 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.121+9276G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326943 | ||||||
| chr7:74326968
|
A | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+9301A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74326968 | ||||||
| chr7:74327342
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.121+9675A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74327342 | ||||||
| chr7:74327507
|
A | C | 122 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0153others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.121+9840A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74327507 | ||||||
| chr7:74327780
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.121+10113C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74327780 | ||||||
| chr7:74327908
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(8): Show | 11 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121+10241G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74327908 | ||||||
| chr7:74328066
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.122-10382G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328066 | ||||||
| chr7:74328094
|
A | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.122-10354A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328094 | ||||||
| chr7:74328193
|
G | A | 2 | a0001c0001t0006g0002a0001c0007t0007g0004 | 2 | HG01074.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.122-10255G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328193 | ||||||
| chr7:74328458
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.122-9990G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328458 | ||||||
| chr7:74328470
|
C | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0017others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-9978C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328470 | ||||||
| chr7:74328820
|
G | A | 1 | a0001c0002t0002g0103 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.122-9628G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328820 | ||||||
| chr7:74328913
|
A | T | 1 | a0001c0002t0005g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.122-9535A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328913 | ||||||
| chr7:74328936
|
A | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.122-9512A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328936 | ||||||
| chr7:74328973
|
T | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.122-9475T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328973 | ||||||
| chr7:74328976
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-9472G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74328976 | ||||||
| chr7:74329087
|
G | GT | 122 | a0001c0001t0001g0104a0001c0001t0001g0137a0001c0001t0001g0155others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.122-9341dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74329087 | |||||
| chr7:74329087
|
G | GTT | 11 | a0001c0001t0001g0171a0001c0002t0001g0090a0001c0002t0001g0115others(8): Show | 11 | HG00735.hp1 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.122-9342_122-9341d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74329087 | |||||
| chr7:74329087
|
GT | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0224others(2): Show | 5 | HG02572.hp1 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-9341delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74329087 | |||||
| chr7:74329090
|
T | G | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.122-9358T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329090 | ||||||
| chr7:74329161
|
C | T | 1 | a0001c0007t0007g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.122-9287C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329161 | ||||||
| chr7:74329215
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-9233C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329215 | ||||||
| chr7:74329267
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122-9181C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329267 | ||||||
| chr7:74329389
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-9059C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329389 | ||||||
| chr7:74329415
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.122-9033C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329415 | ||||||
| chr7:74329516
|
C | T | 1 | a0001c0002t0005g0079 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.122-8932C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329516 | ||||||
| chr7:74329550
|
ATTGT | A | 15 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-8871_122-8868d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74329550 | |||||
| chr7:74329710
|
T | TC | 127 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.122-8738_122-8737i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74329710 | ||||||
| chr7:74329773
|
C | CTATT | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-8658_122-8655d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74329773 | |||||
| chr7:74330138
|
A | G | 113 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.122-8310A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330138 | ||||||
| chr7:74330143
|
G | C | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-8305G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330143 | ||||||
| chr7:74330183
|
C | A | 1 | a0002c0003t0002g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.122-8265C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330183 | ||||||
| chr7:74330248
|
C | CTTT | 106 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.122-8188_122-8186d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74330248 | |||||
| chr7:74330248
|
C | CTTTT | 6 | a0001c0002t0001g0028a0001c0002t0001g0121a0001c0002t0001g0197others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-8189_122-8186d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74330248 | |||||
| chr7:74330291
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.122-8157C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330291 | ||||||
| chr7:74330325
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0002g0046others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-8123C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330325 | ||||||
| chr7:74330556
|
C | T | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.122-7892C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330556 | ||||||
| chr7:74330574
|
T | A | 1 | a0002c0003t0002g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.122-7874T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330574 | ||||||
| chr7:74330605
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122-7843C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330605 | ||||||
| chr7:74330639
|
C | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-7809C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330639 | ||||||
| chr7:74330702
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-7746C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330702 | ||||||
| chr7:74330933
|
T | C | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-7515T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330933 | ||||||
| chr7:74330953
|
C | G | 2 | a0001c0002t0004g0071a0001c0002t0005g0166 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.122-7495C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74330953 | ||||||
| chr7:74331098
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.122-7350C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331098 | ||||||
| chr7:74331205
|
C | CA | 11 | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0129others(8): Show | 11 | HG00642.hp2 HG00673.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.122-7213dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
C | CAA | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02074.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-7214_122-7213d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
C | CAAAAAAA others(6): Show |
1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-7225_122-7213d others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
CA | C | 77 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(74): Show | 77 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.122-7213delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
CAAAA | C | 21 | a0001c0001t0002g0272a0001c0002t0001g0007a0001c0002t0001g0025others(18): Show | 21 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.122-7216_122-7213d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
CAAAAA | C | 87 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.122-7217_122-7213d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331205
|
CAAAAAA | C | 7 | a0001c0002t0001g0094a0001c0002t0001g0099a0001c0002t0001g0121others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-7218_122-7213d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331205 | |||||
| chr7:74331242
|
T | C | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-7206T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331242 | ||||||
| chr7:74331273
|
A | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-7175A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331273 | ||||||
| chr7:74331343
|
A | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-7105A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331343 | ||||||
| chr7:74331360
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122-7088A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331360 | ||||||
| chr7:74331387
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.122-7061A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331387 | ||||||
| chr7:74331400
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-7048G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331400 | ||||||
| chr7:74331418
|
C | G | 1 | a0001c0002t0002g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122-7030C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331418 | ||||||
| chr7:74331562
|
C | CT | 18 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0052others(15): Show | 18 | HG00408.hp2 HG00621.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-6863dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331562 | |||||
| chr7:74331562
|
CT | C | 6 | a0001c0001t0001g0085a0001c0001t0002g0093a0001c0002t0001g0159others(3): Show | 6 | HG01070.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-6863delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74331562 | |||||
| chr7:74331565
|
T | TC | 13 | a0001c0002t0001g0041a0001c0002t0001g0081a0001c0002t0001g0096others(10): Show | 13 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-6883_122-6882i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331565 | ||||||
| chr7:74331566
|
T | C | 96 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.122-6882T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331566 | ||||||
| chr7:74331567
|
T | C | 4 | a0001c0002t0001g0159a0001c0002t0001g0255a0001c0009t0001g0082others(1): Show | 4 | HG01070.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6881T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331567 | ||||||
| chr7:74331609
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-6839G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331609 | ||||||
| chr7:74331635
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-6813G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331635 | ||||||
| chr7:74331801
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.122-6647C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331801 | ||||||
| chr7:74331829
|
T | C | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-6619T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74331829 | ||||||
| chr7:74332000
|
AT | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-6446delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332000 | |||||
| chr7:74332033
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.122-6415G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332033 | ||||||
| chr7:74332136
|
C | T | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.122-6312C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332136 | ||||||
| chr7:74332142
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.122-6306C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332142 | ||||||
| chr7:74332159
|
C | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0017others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-6289C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332159 | ||||||
| chr7:74332223
|
G | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-6225G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332223 | ||||||
| chr7:74332434
|
C | G | 1 | a0001c0004t0002g0001 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.122-6014C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332434 | ||||||
| chr7:74332460
|
C | CTTTT | 5 | a0001c0002t0001g0165a0001c0002t0001g0186a0001c0002t0002g0249others(2): Show | 5 | HG00099.hp1 HG00099.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-5971_122-5968d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332460 | |||||
| chr7:74332460
|
C | CTTTTT | 102 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(99): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.122-5972_122-5968d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332460 | |||||
| chr7:74332460
|
C | CTTTTTT | 9 | a0001c0002t0001g0097a0001c0002t0001g0109a0001c0002t0001g0190others(6): Show | 9 | HG00639.hp1 HG00741.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.122-5973_122-5968d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332460 | |||||
| chr7:74332460
|
CT | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0038others(12): Show | 15 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-5968delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332460 | |||||
| chr7:74332460
|
CTT | C | 48 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(45): Show | 48 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-5969_122-5968d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74332460 | |||||
| chr7:74332462
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.122-5986T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332462 | ||||||
| chr7:74332464
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.122-5984T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332464 | ||||||
| chr7:74332498
|
A | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-5950A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332498 | ||||||
| chr7:74332781
|
A | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-5667A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332781 | ||||||
| chr7:74332786
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-5662G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332786 | ||||||
| chr7:74332817
|
C | T | 1 | a0002c0003t0002g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.122-5631C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332817 | ||||||
| chr7:74332947
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.122-5501C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332947 | ||||||
| chr7:74332972
|
C | T | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.122-5476C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74332972 | ||||||
| chr7:74333277
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0114 | 2 | NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.122-5171G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333277 | ||||||
| chr7:74333311
|
G | A | 51 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-5137G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333311 | ||||||
| chr7:74333380
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-5068C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333380 | ||||||
| chr7:74333407
|
C | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-5041C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333407 | ||||||
| chr7:74333640
|
G | T | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-4808G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333640 | ||||||
| chr7:74333828
|
C | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-4620C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74333828 | ||||||
| chr7:74334125
|
G | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-4323G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334125 | ||||||
| chr7:74334168
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.122-4280T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334168 | ||||||
| chr7:74334223
|
A | G | 51 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-4225A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334223 | ||||||
| chr7:74334299
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-4149G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334299 | ||||||
| chr7:74334705
|
C | T | 1 | a0001c0002t0005g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122-3743C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334705 | ||||||
| chr7:74334823
|
C | CA | 143 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0052others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.122-3609dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74334823 | |||||
| chr7:74334823
|
C | CAA | 10 | a0001c0001t0001g0129a0001c0001t0001g0270a0001c0001t0002g0012others(7): Show | 10 | HG01175.hp1 HG02056.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-3610_122-3609d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74334823 | |||||
| chr7:74334929
|
A | G | 116 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.122-3519A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74334929 | ||||||
| chr7:74335132
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122-3316G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335132 | ||||||
| chr7:74335270
|
C | CA | 18 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(15): Show | 18 | HG01981.hp2 HG02074.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.122-3160dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335270 | |||||
| chr7:74335270
|
C | CAA | 98 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.122-3161_122-3160d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335270 | |||||
| chr7:74335270
|
C | CAAA | 14 | a0001c0002t0001g0105a0001c0002t0001g0139a0001c0002t0001g0170others(11): Show | 14 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-3162_122-3160d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335270 | |||||
| chr7:74335302
|
TGAG | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0233others(1): Show | 4 | HG00438.hp1 HG00609.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3142_122-3140d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335302 | |||||
| chr7:74335347
|
ATTATT | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-3093_122-3089d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335347 | |||||
| chr7:74335502
|
C | CATTT | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-2931_122-2928d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335502 | |||||
| chr7:74335550
|
GGCTGTTC others(2): Show |
G | 49 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(46): Show | 49 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.122-2896_122-2888d others(11): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335550 | |||||
| chr7:74335593
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.122-2855A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335593 | ||||||
| chr7:74335643
|
T | TCCTTCCT others(3): Show |
1 | a0001c0002t0002g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.122-2805_122-2804i others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335643 | ||||||
| chr7:74335643
|
T | TTTCC | 61 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(58): Show | 61 | HG00558.hp2 HG00738.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-2774_122-2771d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335643
|
T | TTTCCTTC others(1): Show |
60 | a0001c0001t0001g0270a0001c0001t0002g0046a0001c0001t0002g0188others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.122-2778_122-2771d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335643
|
T | TTTCCTTC others(5): Show |
27 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0081others(24): Show | 27 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-2782_122-2771d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335643
|
T | TTTCCTTC others(9): Show |
5 | a0001c0002t0001g0028a0001c0002t0001g0099a0001c0002t0001g0139others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-2786_122-2771d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335643
|
TTTCC | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG02559.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.122-2774_122-2771d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335643
|
TTTCCTTC others(1): Show |
T | 3 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122-2778_122-2771d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335643 | |||||
| chr7:74335658
|
CCTTCCTT others(13): Show |
C | 2 | a0001c0002t0001g0234a0001c0002t0002g0238 | 2 | NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.122-2778_122-2759d others(22): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335658 | |||||
| chr7:74335662
|
CCTTCCTT others(9): Show |
C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-2774_122-2759d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335662 | |||||
| chr7:74335670
|
CCTTCCTT others(1): Show |
C | 4 | a0001c0002t0001g0097a0001c0002t0001g0161a0001c0002t0001g0248others(1): Show | 4 | HG00639.hp2 HG01074.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-2770_122-2763d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335670 | |||||
| chr7:74335678
|
G | C | 107 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.122-2770G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335678 | ||||||
| chr7:74335690
|
T | C | 2 | a0001c0002t0001g0102a0001c0002t0001g0121 | 2 | HG00323.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.122-2758T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335690 | ||||||
| chr7:74335724
|
CCTTTCTT others(6): Show |
C | 1 | a0001c0004t0002g0132 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.122-2706_122-2694d others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74335724 | |||||
| chr7:74335804
|
G | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-2644G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335804 | ||||||
| chr7:74335956
|
T | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-2492T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335956 | ||||||
| chr7:74335991
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-2457C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74335991 | ||||||
| chr7:74336012
|
GATT | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-2434_122-2432d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336012 | |||||
| chr7:74336069
|
A | ATTATT | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.122-2377_122-2376i others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336069 | |||||
| chr7:74336156
|
C | T | 30 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(27): Show | 30 | HG00558.hp2 HG01884.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.122-2292C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336156 | ||||||
| chr7:74336172
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-2276A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336172 | ||||||
| chr7:74336240
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-2208G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336240 | ||||||
| chr7:74336347
|
C | T | 115 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.122-2101C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336347 | ||||||
| chr7:74336472
|
A | G | 5 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0017others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-1976A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336472 | ||||||
| chr7:74336476
|
C | T | 117 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.122-1972C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336476 | ||||||
| chr7:74336498
|
G | A | 2 | a0001c0002t0001g0204a0001c0002t0001g0217 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122-1950G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336498 | ||||||
| chr7:74336607
|
C | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-1841C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336607 | ||||||
| chr7:74336730
|
A | G | 12 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0174others(9): Show | 12 | HG00558.hp1 HG00673.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.122-1718A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336730 | ||||||
| chr7:74336772
|
A | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-1676A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336772 | ||||||
| chr7:74336847
|
GTTTGTTT others(8): Show |
G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-1597_122-1583d others(17): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336847 | |||||
| chr7:74336860
|
G | GT | 7 | a0001c0001t0001g0020a0001c0001t0001g0076a0001c0001t0001g0137others(4): Show | 7 | HG00609.hp2 HG01074.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-1574dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336860 | |||||
| chr7:74336860
|
G | T | 1 | a0002c0003t0004g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.122-1588G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336860 | ||||||
| chr7:74336860
|
GT | G | 51 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-1574delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336860 | |||||
| chr7:74336870
|
T | TG | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-1578_122-1577i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336870 | ||||||
| chr7:74336871
|
T | G | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-1577T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336871 | ||||||
| chr7:74336880
|
T | G | 115 | a0001c0001t0001g0104a0001c0001t0001g0144a0001c0001t0001g0268others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.122-1568T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336880 | ||||||
| chr7:74336885
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122-1563G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336885 | ||||||
| chr7:74336888
|
TTG | T | 113 | a0001c0001t0001g0104a0001c0001t0001g0189a0001c0001t0001g0268others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.122-1558_122-1557d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336888 | |||||
| chr7:74336890
|
GT | G | 146 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 146 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.122-1545delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74336890 | |||||
| chr7:74336891
|
T | G | 112 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.122-1557T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336891 | ||||||
| chr7:74336895
|
T | G | 1 | a0001c0002t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122-1553T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336895 | ||||||
| chr7:74336912
|
G | A | 114 | a0001c0001t0001g0104a0001c0001t0001g0268a0001c0001t0001g0270others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.122-1536G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336912 | ||||||
| chr7:74336920
|
C | G | 51 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.122-1528C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74336920 | ||||||
| chr7:74337062
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.122-1386A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337062 | ||||||
| chr7:74337076
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG02559.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-1372C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337076 | ||||||
| chr7:74337386
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-1062G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337386 | ||||||
| chr7:74337422
|
C | T | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-1026C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337422 | ||||||
| chr7:74337508
|
G | T | 6 | a0001c0002t0001g0141a0001c0002t0001g0159a0001c0002t0001g0163others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-940G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337508 | ||||||
| chr7:74337509
|
G | A | 1 | a0001c0002t0002g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122-939G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337509 | ||||||
| chr7:74337593
|
C | CTT | 106 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.122-845_122-844dup others(2): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74337593 | |||||
| chr7:74337593
|
CT | C | 54 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.122-844delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 74337593 | |||||
| chr7:74337787
|
G | A | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.122-661G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74337787 | ||||||
| chr7:74338194
|
C | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0195 | 2 | HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.122-254C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338194 | ||||||
| chr7:74338212
|
T | C | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.122-236T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338212 | ||||||
| chr7:74338216
|
CAG | C | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.122-231_122-230del others(2): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338216 | ||||||
| chr7:74338277
|
G | A | 49 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(46): Show | 49 | HG00558.hp2 HG00735.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.122-171G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338277 | ||||||
| chr7:74338317
|
G | C | 111 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.122-131G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338317 | ||||||
| chr7:74338369
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.122-79C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 2/16 | chr7 | 74338369 | ||||||
| chr7:74339054
|
T | A | 1 | a0001c0002t0001g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.678+50T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339054 | ||||||
| chr7:74339155
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.678+151C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339155 | ||||||
| chr7:74339298
|
C | CTTAT | 40 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.678+313_678+316dup others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74339298 | |||||
| chr7:74339298
|
C | CTTATTTA others(5): Show |
62 | a0001c0002t0001g0081a0001c0002t0001g0088a0001c0002t0001g0090others(59): Show | 62 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.678+305_678+316dup others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74339298 | |||||
| chr7:74339298
|
C | CTTATTTA others(9): Show |
5 | a0001c0002t0001g0091a0001c0002t0001g0181a0001c0002t0001g0239others(2): Show | 5 | HG00609.hp1 HG03831.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+301_678+316dup others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74339298 | |||||
| chr7:74339298
|
C | CTTATTTA others(13): Show |
2 | a0001c0002t0001g0161a0001c0018t0001g0095 | 2 | HG00639.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.678+297_678+316dup others(20): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74339298 | |||||
| chr7:74339298
|
CTTAT | C | 2 | a0001c0001t0001g0143a0007c0017t0004g0075 | 2 | HG01258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.678+313_678+316del others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74339298 | |||||
| chr7:74339402
|
T | A | 11 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(8): Show | 11 | HG01433.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.678+398T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339402 | ||||||
| chr7:74339425
|
C | A | 5 | a0001c0004t0001g0107a0001c0004t0002g0001a0001c0004t0002g0128others(2): Show | 5 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+421C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339425 | ||||||
| chr7:74339462
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+458C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339462 | ||||||
| chr7:74339565
|
C | T | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.678+561C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339565 | ||||||
| chr7:74339657
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.678+653G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339657 | ||||||
| chr7:74339696
|
T | C | 1 | a0002c0003t0002g0183 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.678+692T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339696 | ||||||
| chr7:74339940
|
C | A | 111 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.678+936C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339940 | ||||||
| chr7:74339981
|
C | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+977C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74339981 | ||||||
| chr7:74340131
|
C | T | 1 | a0001c0002t0016g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.678+1127C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340131 | ||||||
| chr7:74340257
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.678+1253G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340257 | ||||||
| chr7:74340265
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+1261G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340265 | ||||||
| chr7:74340293
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.678+1289A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340293 | ||||||
| chr7:74340419
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.678+1415G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340419 | ||||||
| chr7:74340768
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+1764C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340768 | ||||||
| chr7:74340808
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+1804G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340808 | ||||||
| chr7:74340930
|
G | C | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+1926G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74340930 | ||||||
| chr7:74341068
|
T | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+2064T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341068 | ||||||
| chr7:74341069
|
A | G | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.678+2065A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341069 | ||||||
| chr7:74341128
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+2124G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341128 | ||||||
| chr7:74341241
|
G | A | 1 | a0008c0021t0001g0136 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.678+2237G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341241 | ||||||
| chr7:74341440
|
A | G | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+2436A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341440 | ||||||
| chr7:74341597
|
C | CT | 63 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(60): Show | 63 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.678+2607dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74341597 | |||||
| chr7:74341619
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+2615G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341619 | ||||||
| chr7:74341810
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.678+2806G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341810 | ||||||
| chr7:74341970
|
G | A | 1 | a0001c0002t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.678+2966G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74341970 | ||||||
| chr7:74342307
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+3303C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342307 | ||||||
| chr7:74342332
|
C | T | 2 | a0001c0001t0003g0070a0001c0014t0003g0060 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.678+3328C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342332 | ||||||
| chr7:74342375
|
C | CA | 57 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(54): Show | 57 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.678+3381dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74342375 | |||||
| chr7:74342386
|
CA | C | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+3391delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74342386 | |||||
| chr7:74342455
|
T | C | 240 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.678+3451T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342455 | ||||||
| chr7:74342646
|
G | C | 1 | a0001c0002t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.678+3642G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342646 | ||||||
| chr7:74342712
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.678+3708A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342712 | ||||||
| chr7:74342863
|
G | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(4): Show | 7 | HG01099.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.678+3859G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74342863 | ||||||
| chr7:74343034
|
C | CA | 130 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 130 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.678+4045dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74343034 | |||||
| chr7:74343151
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.678+4147C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343151 | ||||||
| chr7:74343183
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.678+4179G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343183 | ||||||
| chr7:74343301
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.678+4297G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343301 | ||||||
| chr7:74343385
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.678+4381T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343385 | ||||||
| chr7:74343401
|
C | T | 1 | a0001c0002t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.678+4397C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343401 | ||||||
| chr7:74343426
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+4422G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343426 | ||||||
| chr7:74343491
|
CTTCA | C | 4 | a0001c0002t0001g0028a0001c0002t0001g0205a0001c0002t0001g0214others(1): Show | 4 | HG02922.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+4515_678+4518d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74343491 | |||||
| chr7:74343630
|
T | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.678+4626T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343630 | ||||||
| chr7:74343738
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0150a0001c0001t0006g0014others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+4750delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74343738 | |||||
| chr7:74343738
|
CAA | C | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+4749_678+4750d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74343738 | |||||
| chr7:74343824
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+4820G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343824 | ||||||
| chr7:74343853
|
C | T | 1 | a0006c0013t0002g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.678+4849C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343853 | ||||||
| chr7:74343865
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+4861C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74343865 | ||||||
| chr7:74344088
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.678+5084G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344088 | ||||||
| chr7:74344133
|
T | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.678+5129T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344133 | ||||||
| chr7:74344235
|
G | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+5231G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344235 | ||||||
| chr7:74344286
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.678+5282G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344286 | ||||||
| chr7:74344482
|
A | G | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+5478A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344482 | ||||||
| chr7:74344640
|
C | T | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.678+5636C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344640 | ||||||
| chr7:74344847
|
C | T | 37 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.678+5843C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74344847 | ||||||
| chr7:74345214
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+6210G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345214 | ||||||
| chr7:74345384
|
G | A | 4 | a0001c0002t0001g0088a0001c0002t0001g0197a0001c0002t0001g0250others(1): Show | 4 | NA18952.hp2 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+6380G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345384 | ||||||
| chr7:74345455
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.678+6451A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345455 | ||||||
| chr7:74345493
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+6489G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345493 | ||||||
| chr7:74345646
|
G | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.678+6642G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345646 | ||||||
| chr7:74345697
|
A | C | 1 | a0001c0002t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.678+6693A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345697 | ||||||
| chr7:74345739
|
C | A | 2 | a0001c0019t0007g0142a0001c0020t0006g0267 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.678+6735C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345739 | ||||||
| chr7:74345778
|
C | T | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.678+6774C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74345778 | ||||||
| chr7:74346249
|
G | A | 1 | a0001c0002t0005g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.678+7245G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346249 | ||||||
| chr7:74346305
|
G | C | 1 | a0002c0003t0002g0183 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.678+7301G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346305 | ||||||
| chr7:74346374
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.678+7370G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346374 | ||||||
| chr7:74346448
|
C | T | 4 | a0001c0002t0001g0028a0001c0002t0001g0205a0001c0002t0001g0214others(1): Show | 4 | HG02922.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-7432C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346448 | ||||||
| chr7:74346544
|
A | G | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.679-7336A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346544 | ||||||
| chr7:74346552
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.679-7328G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346552 | ||||||
| chr7:74346635
|
G | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.679-7245G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346635 | ||||||
| chr7:74346718
|
C | CA | 13 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0143others(10): Show | 13 | HG01258.hp2 HG01981.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.679-7138dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74346718 | |||||
| chr7:74346729
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.679-7151A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346729 | ||||||
| chr7:74346730
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.679-7150A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346730 | ||||||
| chr7:74346731
|
AAAAAAAA others(5): Show |
A | 68 | a0001c0002t0001g0081a0001c0002t0001g0088a0001c0002t0001g0090others(65): Show | 68 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.679-7144_679-7133d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74346731 | |||||
| chr7:74346732
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0002t0001g0094a0001c0002t0002g0119 | 2 | HG02155.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.679-7143_679-7133d others(13): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74346732 | |||||
| chr7:74346735
|
A | C | 56 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(53): Show | 56 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.679-7145A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346735 | ||||||
| chr7:74346738
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.679-7142A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346738 | ||||||
| chr7:74346739
|
AAAAC | A | 27 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0028others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.679-7137_679-7134d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74346739 | |||||
| chr7:74346740
|
AAAC | A | 10 | a0001c0002t0001g0024a0001c0002t0001g0141a0001c0002t0001g0167others(7): Show | 10 | HG00733.hp2 HG01168.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.679-7137_679-7135d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74346740 | |||||
| chr7:74346743
|
C | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0008t0009g0031others(1): Show | 4 | HG00140.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-7137C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346743 | ||||||
| chr7:74346786
|
C | A | 109 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.679-7094C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346786 | ||||||
| chr7:74346908
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.679-6972G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74346908 | ||||||
| chr7:74347061
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.679-6819G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347061 | ||||||
| chr7:74347087
|
G | A | 3 | a0001c0004t0001g0107a0001c0004t0002g0001a0001c0004t0002g0132 | 3 | HG02071.hp2 HG02074.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.679-6793G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347087 | ||||||
| chr7:74347312
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.679-6568A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347312 | ||||||
| chr7:74347369
|
C | T | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.679-6511C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347369 | ||||||
| chr7:74347395
|
G | A | 179 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.679-6485G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347395 | ||||||
| chr7:74347520
|
G | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.679-6360G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347520 | ||||||
| chr7:74347558
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.679-6322G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347558 | ||||||
| chr7:74347561
|
T | C | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(5): Show | 8 | HG01099.hp2 HG01433.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.679-6319T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347561 | ||||||
| chr7:74347582
|
C | CT | 7 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0108others(4): Show | 7 | HG00408.hp2 HG02083.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.679-6297dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74347582 | |||||
| chr7:74347625
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.679-6255C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347625 | ||||||
| chr7:74347639
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.679-6241T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347639 | ||||||
| chr7:74347644
|
A | G | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.679-6236A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347644 | ||||||
| chr7:74347949
|
A | G | 107 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.679-5931A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347949 | ||||||
| chr7:74347978
|
C | G | 107 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.679-5902C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74347978 | ||||||
| chr7:74348073
|
G | A | 1 | a0001c0002t0016g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.679-5807G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348073 | ||||||
| chr7:74348228
|
G | A | 1 | a0001c0002t0018g0256 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.679-5652G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348228 | ||||||
| chr7:74348348
|
A | C | 1 | a0001c0002t0001g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.679-5532A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348348 | ||||||
| chr7:74348554
|
C | T | 1 | a0001c0002t0001g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.679-5326C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348554 | ||||||
| chr7:74348715
|
A | G | 1 | a0001c0002t0005g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.679-5165A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348715 | ||||||
| chr7:74348768
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.679-5112C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348768 | ||||||
| chr7:74348769
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.679-5111A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348769 | ||||||
| chr7:74348777
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.679-5103G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348777 | ||||||
| chr7:74348789
|
C | CA | 107 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0001g0268others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.679-5073dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74348789 | |||||
| chr7:74348840
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.679-5040G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348840 | ||||||
| chr7:74348941
|
G | T | 1 | a0001c0002t0001g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.679-4939G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348941 | ||||||
| chr7:74348978
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679-4902C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348978 | ||||||
| chr7:74348995
|
T | A | 37 | a0001c0002t0001g0081a0001c0002t0001g0088a0001c0002t0001g0090others(34): Show | 37 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.679-4885T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74348995 | ||||||
| chr7:74349052
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.679-4828G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349052 | ||||||
| chr7:74349064
|
A | G | 108 | a0001c0001t0001g0053a0001c0002t0001g0007a0001c0002t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-4816A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349064 | ||||||
| chr7:74349135
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.679-4745A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349135 | ||||||
| chr7:74349159
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.679-4721A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349159 | ||||||
| chr7:74349168
|
T | C | 1 | a0007c0017t0004g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.679-4712T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349168 | ||||||
| chr7:74349208
|
A | G | 233 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.679-4672A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349208 | ||||||
| chr7:74349429
|
C | CA | 11 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0154others(8): Show | 11 | HG00673.hp2 HG01099.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-4433dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349429 | |||||
| chr7:74349429
|
CA | C | 69 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0020others(66): Show | 69 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.679-4433delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349429 | |||||
| chr7:74349447
|
A | AAT | 6 | a0001c0002t0001g0106a0001c0002t0001g0159a0001c0002t0001g0255others(3): Show | 6 | HG01978.hp2 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-4433_679-4432i others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349447 | ||||||
| chr7:74349447
|
A | AT | 97 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.679-4433_679-4432i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349447 | ||||||
| chr7:74349447
|
A | T | 10 | a0001c0001t0001g0053a0001c0002t0001g0028a0001c0002t0001g0204others(7): Show | 10 | HG02602.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.679-4433A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349447 | ||||||
| chr7:74349454
|
A | G | 4 | a0001c0002t0001g0161a0001c0002t0001g0247a0001c0002t0001g0248others(1): Show | 4 | HG00639.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-4426A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349454 | ||||||
| chr7:74349454
|
ATG | A | 17 | a0001c0002t0001g0007a0001c0002t0001g0101a0001c0002t0001g0106others(14): Show | 17 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.679-4410_679-4409d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349454 | |||||
| chr7:74349458
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG00733.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-4422G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349458 | ||||||
| chr7:74349466
|
GTGTGTAT others(15): Show |
G | 6 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG02630.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.679-4412_679-4391d others(24): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349466 | |||||
| chr7:74349468
|
G | GTA | 41 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0219others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(38): Show |
intron_variant | MODIFIER | c.679-4411_679-4410i others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
G | GTATA | 11 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0001t0001g0156others(8): Show | 11 | HG01258.hp1 HG03017.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.679-4411_679-4410i others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
G | GTATATA | 5 | a0001c0001t0001g0271a0001c0001t0006g0014a0001c0002t0001g0250others(2): Show | 5 | HG02738.hp1 HG03225.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-4411_679-4410i others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
G | GTATATAT others(3): Show |
1 | a0001c0002t0001g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.679-4411_679-4410i others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.679-4411_679-4410i others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
G | GTATATAT others(11): Show |
1 | a0002c0003t0002g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.679-4411_679-4410i others(20): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
GTGTATAT others(9): Show |
G | 2 | a0001c0008t0009g0149a0001c0008t0009g0211 | 2 | HG01192.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.679-4410_679-4395d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
GTGTATAT others(13): Show |
G | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.679-4410_679-4391d others(22): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
GTGTATAT others(17): Show |
G | 2 | a0001c0002t0001g0139a0002c0003t0002g0116 | 2 | HG03516.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.679-4410_679-4387d others(26): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
GTGTATAT others(19): Show |
G | 4 | a0001c0019t0007g0142a0001c0020t0006g0267a0002c0003t0002g0049others(1): Show | 4 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-4410_679-4385d others(28): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349468
|
GTGTATAT others(21): Show |
G | 2 | a0001c0002t0001g0118a0001c0002t0001g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.679-4410_679-4383d others(30): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349468 | |||||
| chr7:74349470
|
G | A | 105 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.679-4410G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349470 | ||||||
| chr7:74349470
|
G | GTA | 22 | a0001c0001t0001g0008a0001c0001t0001g0087a0001c0001t0001g0143others(19): Show | 22 | HG00140.hp2 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.679-4370_679-4369d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
G | GTATA | 19 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0144others(16): Show | 19 | HG01928.hp1 HG01943.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.679-4372_679-4369d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0076a0001c0001t0002g0259a0001c0001t0002g0263others(1): Show | 4 | HG00741.hp1 HG01070.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-4376_679-4369d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.679-4378_679-4369d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
G | GTGTATA | 4 | a0001c0001t0003g0070a0001c0004t0002g0128a0001c0004t0002g0175others(1): Show | 4 | HG00558.hp1 HG00673.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-4409_679-4408i others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTA | G | 23 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 23 | HG00733.hp1 HG01243.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.679-4370_679-4369d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATA | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0180a0001c0001t0002g0093others(3): Show | 6 | HG03195.hp1 HG03492.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-4372_679-4369d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATA | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0003g0064others(2): Show | 5 | HG00735.hp2 HG01978.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-4374_679-4369d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0003g0059 | 3 | HG02622.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.679-4376_679-4369d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(5): Show |
G | 4 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0233others(1): Show | 4 | HG00438.hp1 HG00741.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-4380_679-4369d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(7): Show |
G | 7 | a0001c0001t0001g0078a0001c0001t0001g0114a0001c0001t0002g0022others(4): Show | 7 | HG00609.hp2 NA18940.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-4382_679-4369d others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0002g0188a0001c0001t0003g0063a0002c0003t0002g0183 | 3 | NA18952.hp1 NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.679-4384_679-4369d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.679-4390_679-4369d others(24): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0011a0001c0001t0001g0202 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.679-4392_679-4369d others(26): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349470
|
GTATATAT others(21): Show |
G | 1 | a0001c0002t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.679-4396_679-4369d others(30): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349470 | |||||
| chr7:74349472
|
A | G | 2 | a0001c0002t0001g0225a0002c0003t0002g0203 | 2 | HG00733.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.679-4408A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349472 | ||||||
| chr7:74349474
|
A | G | 2 | a0001c0001t0004g0057a0002c0003t0002g0203 | 2 | HG02132.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.679-4406A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349474 | ||||||
| chr7:74349476
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0003g0056 | 2 | HG03492.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.679-4404A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349476 | ||||||
| chr7:74349486
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0005g0018 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.679-4391_679-4366d others(28): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74349486 | |||||
| chr7:74349512
|
G | A | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.679-4368G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349512 | ||||||
| chr7:74349618
|
T | C | 4 | a0001c0002t0001g0118a0001c0002t0001g0131a0001c0002t0001g0213others(1): Show | 4 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-4262T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349618 | ||||||
| chr7:74349697
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.679-4183A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349697 | ||||||
| chr7:74349737
|
C | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.679-4143C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349737 | ||||||
| chr7:74349948
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.679-3932G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74349948 | ||||||
| chr7:74350140
|
G | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0020others(63): Show | 66 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.679-3740G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350140 | ||||||
| chr7:74350144
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-3736C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350144 | ||||||
| chr7:74350155
|
G | A | 1 | a0001c0004t0002g0128 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.679-3725G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350155 | ||||||
| chr7:74350388
|
A | G | 177 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.679-3492A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350388 | ||||||
| chr7:74350408
|
A | G | 2 | a0001c0001t0003g0070a0001c0014t0003g0060 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.679-3472A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350408 | ||||||
| chr7:74350439
|
C | T | 108 | a0001c0001t0001g0053a0001c0002t0001g0007a0001c0002t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-3441C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350439 | ||||||
| chr7:74350452
|
C | T | 53 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.679-3428C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350452 | ||||||
| chr7:74350508
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.679-3372C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350508 | ||||||
| chr7:74350706
|
A | T | 54 | a0001c0001t0001g0047a0001c0001t0001g0085a0001c0001t0001g0086others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.679-3174A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350706 | ||||||
| chr7:74350886
|
GAA | G | 53 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.679-2992_679-2991d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74350886 | |||||
| chr7:74350919
|
G | GGGAAGGA others(2): Show |
52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.679-2953_679-2952i others(11): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74350919 | |||||
| chr7:74350919
|
GGGAAGGA others(11): Show |
G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.679-2947_679-2930d others(20): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74350919 | |||||
| chr7:74350921
|
G | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-2959G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350921 | ||||||
| chr7:74350933
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.679-2947G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74350933 | ||||||
| chr7:74351002
|
GAGAA | G | 54 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.679-2869_679-2866d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351002 | |||||
| chr7:74351006
|
A | AAGAAAG | 117 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.679-2872_679-2867d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351006 | |||||
| chr7:74351019
|
G | A | 1 | a0001c0002t0001g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.679-2861G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351019 | ||||||
| chr7:74351030
|
A | G | 1 | a0001c0002t0001g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.679-2850A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351030 | ||||||
| chr7:74351031
|
G | A | 1 | a0001c0002t0001g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.679-2849G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351031 | ||||||
| chr7:74351065
|
GAGAA | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 70 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.679-2797_679-2794d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351065 | |||||
| chr7:74351081
|
AAGAAAAA others(1): Show |
A | 108 | a0001c0001t0001g0053a0001c0002t0001g0007a0001c0002t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-2797_679-2790d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351081 | |||||
| chr7:74351092
|
G | A | 108 | a0001c0001t0001g0053a0001c0002t0001g0007a0001c0002t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-2788G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351092 | ||||||
| chr7:74351133
|
A | AAG | 22 | a0001c0002t0001g0117a0001c0002t0001g0121a0001c0002t0001g0122others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.679-2729_679-2728d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351133 | |||||
| chr7:74351153
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0002g0006 | 2 | HG00558.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.679-2727A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351153 | ||||||
| chr7:74351264
|
C | G | 1 | a0001c0002t0001g0245 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.679-2616C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351264 | ||||||
| chr7:74351426
|
C | CA | 127 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(124): Show | 127 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.679-2432dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351426 | |||||
| chr7:74351426
|
CA | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG01099.hp1 HG01106.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-2432delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74351426 | |||||
| chr7:74351602
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.679-2278A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351602 | ||||||
| chr7:74351729
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.679-2151C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351729 | ||||||
| chr7:74351749
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-2131C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351749 | ||||||
| chr7:74351758
|
C | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.679-2122C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351758 | ||||||
| chr7:74351899
|
A | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-1981A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351899 | ||||||
| chr7:74351927
|
G | T | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.679-1953G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351927 | ||||||
| chr7:74351948
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-1932T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74351948 | ||||||
| chr7:74352028
|
G | A | 1 | a0001c0010t0003g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.679-1852G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352028 | ||||||
| chr7:74352189
|
C | T | 7 | a0001c0002t0001g0170a0001c0002t0001g0190a0001c0002t0001g0199others(4): Show | 7 | HG00408.hp1 HG02071.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.679-1691C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352189 | ||||||
| chr7:74352229
|
G | C | 1 | a0001c0002t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.679-1651G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352229 | ||||||
| chr7:74352338
|
G | T | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.679-1542G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352338 | ||||||
| chr7:74352396
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.679-1484C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352396 | ||||||
| chr7:74352415
|
C | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-1465C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352415 | ||||||
| chr7:74352426
|
G | C | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.679-1454G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352426 | ||||||
| chr7:74352482
|
A | C | 54 | a0001c0001t0001g0047a0001c0001t0001g0085a0001c0001t0001g0086others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.679-1398A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352482 | ||||||
| chr7:74352641
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-1239C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352641 | ||||||
| chr7:74352650
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-1230G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352650 | ||||||
| chr7:74352698
|
C | CAA | 9 | a0001c0001t0001g0039a0001c0001t0003g0059a0001c0002t0001g0159others(6): Show | 9 | HG00099.hp1 HG01071.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.679-1168_679-1167d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74352698 | |||||
| chr7:74352698
|
C | CAAA | 108 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.679-1169_679-1167d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74352698 | |||||
| chr7:74352698
|
CA | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0180a0001c0001t0002g0264others(4): Show | 7 | HG01070.hp1 HG01081.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-1167delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74352698 | |||||
| chr7:74352714
|
T | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-1166T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74352714 | ||||||
| chr7:74353253
|
C | CT | 6 | a0001c0001t0001g0008a0001c0001t0001g0224a0001c0002t0001g0024others(3): Show | 6 | HG00741.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-612dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74353253 | |||||
| chr7:74353253
|
CT | C | 7 | a0001c0002t0001g0081a0001c0002t0001g0096a0001c0002t0001g0159others(4): Show | 7 | HG01081.hp1 HG01496.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-612delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 74353253 | |||||
| chr7:74353315
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.679-565A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74353315 | ||||||
| chr7:74353411
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.679-469C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74353411 | ||||||
| chr7:74353508
|
C | T | 2 | a0001c0001t0001g0224a0001c0008t0009g0031 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.679-372C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74353508 | ||||||
| chr7:74353541
|
A | G | 1 | a0001c0002t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.679-339A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74353541 | ||||||
| chr7:74353735
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.679-145T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 3/16 | chr7 | 74353735 | ||||||
| chr7:74354061
|
G | A | 1 | a0001c0001t0002g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.803+57G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354061 | ||||||
| chr7:74354116
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0233others(1): Show | 4 | HG00438.hp1 HG00609.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+112A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354116 | ||||||
| chr7:74354234
|
C | A | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.803+230C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354234 | ||||||
| chr7:74354523
|
G | A | 2 | a0001c0001t0001g0224a0001c0008t0009g0031 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.803+519G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354523 | ||||||
| chr7:74354547
|
G | A | 108 | a0001c0001t0001g0053a0001c0002t0001g0007a0001c0002t0001g0024others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.803+543G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354547 | ||||||
| chr7:74354637
|
G | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.803+633G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354637 | ||||||
| chr7:74354695
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.803+691C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354695 | ||||||
| chr7:74354728
|
G | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0051a0002c0003t0002g0177 | 3 | HG01243.hp1 HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.803+724G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354728 | ||||||
| chr7:74354729
|
C | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0051a0002c0003t0002g0177 | 3 | HG01243.hp1 HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.803+725C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74354729 | ||||||
| chr7:74354783
|
A | AAAAT | 5 | a0001c0001t0001g0053a0001c0001t0008g0029a0001c0002t0001g0204others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+799_803+802dup others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 74354783 | |||||
| chr7:74355129
|
T | C | 243 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.803+1125T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74355129 | ||||||
| chr7:74355470
|
C | A | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.804-940C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74355470 | ||||||
| chr7:74355565
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.804-845G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74355565 | ||||||
| chr7:74355690
|
C | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.804-720C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74355690 | ||||||
| chr7:74356017
|
G | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-393G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 4/16 | chr7 | 74356017 | ||||||
| chr7:74356718
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1017+95C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 5/16 | chr7 | 74356718 | ||||||
| chr7:74357525
|
T | C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1215+48T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74357525 | ||||||
| chr7:74357763
|
CT | C | 6 | a0001c0001t0002g0111a0001c0001t0006g0016a0001c0002t0001g0105others(3): Show | 6 | HG00639.hp2 HG01943.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+299delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74357763 | |||||
| chr7:74357825
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1215+348C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74357825 | ||||||
| chr7:74357908
|
C | T | 1 | a0001c0010t0003g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1215+431C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74357908 | ||||||
| chr7:74357998
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1215+521A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74357998 | ||||||
| chr7:74358051
|
G | GT | 29 | a0001c0001t0001g0078a0001c0001t0001g0114a0001c0001t0001g0155others(26): Show | 29 | HG00621.hp1 HG00639.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1215+590dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74358051 | |||||
| chr7:74358068
|
A | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1215+591A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358068 | ||||||
| chr7:74358075
|
A | G | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1215+598A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358075 | ||||||
| chr7:74358082
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1215+605C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358082 | ||||||
| chr7:74358161
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1215+684C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358161 | ||||||
| chr7:74358297
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1215+820T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358297 | ||||||
| chr7:74358387
|
G | A | 8 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0113others(5): Show | 8 | HG01258.hp1 HG02132.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1215+910G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358387 | ||||||
| chr7:74358413
|
C | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1215+936C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358413 | ||||||
| chr7:74358422
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1215+945G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358422 | ||||||
| chr7:74358568
|
CT | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1215+1103delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74358568 | |||||
| chr7:74358617
|
T | C | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1215+1140T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358617 | ||||||
| chr7:74358627
|
G | A | 12 | a0001c0002t0001g0170a0001c0002t0001g0190a0001c0002t0001g0199others(9): Show | 12 | HG00408.hp1 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+1150G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358627 | ||||||
| chr7:74358674
|
A | G | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(4): Show | 7 | HG01099.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+1197A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358674 | ||||||
| chr7:74358841
|
G | A | 1 | a0001c0001t0004g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1216-1334G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74358841 | ||||||
| chr7:74359084
|
G | A | 2 | a0001c0002t0004g0071a0001c0002t0005g0166 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1216-1091G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359084 | ||||||
| chr7:74359086
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1216-1089C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359086 | ||||||
| chr7:74359221
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1216-954G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359221 | ||||||
| chr7:74359224
|
C | T | 2 | a0003c0005t0002g0173a0003c0005t0002g0179 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1216-951C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359224 | ||||||
| chr7:74359228
|
C | T | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1216-947C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359228 | ||||||
| chr7:74359304
|
C | CT | 12 | a0001c0001t0001g0224a0001c0001t0002g0263a0001c0001t0006g0014others(9): Show | 12 | HG00639.hp1 HG00741.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1216-854dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74359304 | |||||
| chr7:74359304
|
CT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0047others(8): Show | 11 | HG00099.hp1 HG01081.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1216-854delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74359304 | |||||
| chr7:74359350
|
C | CT | 61 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(58): Show | 61 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1216-811dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 74359350 | |||||
| chr7:74359416
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1216-759T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359416 | ||||||
| chr7:74359515
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1216-660A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359515 | ||||||
| chr7:74359545
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0033others(12): Show | 15 | HG01071.hp2 HG01074.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1216-630T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359545 | ||||||
| chr7:74359548
|
G | A | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1216-627G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359548 | ||||||
| chr7:74359557
|
A | G | 4 | a0001c0002t0002g0119a0001c0002t0002g0158a0004c0016t0001g0212others(1): Show | 4 | HG02886.hp1 NA18940.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-618A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359557 | ||||||
| chr7:74359577
|
A | G | 16 | a0001c0001t0002g0006a0001c0002t0001g0094a0001c0002t0001g0106others(13): Show | 16 | HG00408.hp1 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1216-598A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359577 | ||||||
| chr7:74359606
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1216-569T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359606 | ||||||
| chr7:74359635
|
A | G | 1 | a0001c0002t0001g0105 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1216-540A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359635 | ||||||
| chr7:74359636
|
G | T | 1 | a0001c0002t0001g0105 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1216-539G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359636 | ||||||
| chr7:74359644
|
T | C | 1 | a0001c0002t0001g0237 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1216-531T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359644 | ||||||
| chr7:74359663
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1216-512A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 6/16 | chr7 | 74359663 | ||||||
| chr7:74360695
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1319+417C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74360695 | ||||||
| chr7:74360829
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1319+551G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74360829 | ||||||
| chr7:74360959
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1319+681G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74360959 | ||||||
| chr7:74361091
|
T | C | 1 | a0001c0002t0001g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1319+813T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361091 | ||||||
| chr7:74361136
|
A | T | 1 | a0001c0002t0018g0256 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1319+858A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361136 | ||||||
| chr7:74361176
|
T | TTTCC | 13 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0111others(10): Show | 13 | HG00140.hp2 HG01099.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1319+927_1319+930d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(1): Show |
89 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0037others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1319+923_1319+930d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(5): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0086a0001c0001t0001g0154others(8): Show | 11 | HG00609.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1319+919_1319+930d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(9): Show |
8 | a0001c0001t0001g0036a0001c0001t0001g0155a0001c0001t0003g0059others(5): Show | 8 | HG00323.hp1 HG02074.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1319+915_1319+930d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(13): Show |
19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 19 | HG00099.hp1 HG00733.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.1319+911_1319+930d others(22): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(17): Show |
18 | a0001c0001t0001g0021a0001c0001t0001g0224a0001c0001t0002g0006others(15): Show | 18 | HG00558.hp2 HG00738.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1319+907_1319+930d others(26): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(21): Show |
26 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0092others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319+903_1319+930d others(30): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(25): Show |
40 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0274others(37): Show | 40 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.1319+899_1319+930d others(34): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(29): Show |
14 | a0001c0001t0001g0087a0001c0002t0001g0024a0001c0002t0001g0025others(11): Show | 14 | HG00408.hp1 HG00639.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1319+930_1319+931i others(38): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(33): Show |
5 | a0001c0002t0001g0097a0001c0002t0001g0105a0001c0002t0001g0118others(2): Show | 5 | HG00621.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319+930_1319+931i others(42): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
T | TTTCCTTC others(62): Show |
1 | a0001c0001t0001g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1319+930_1319+931i others(71): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361176
|
TTTCC | T | 5 | a0001c0001t0001g0144a0001c0001t0002g0134a0001c0001t0006g0002others(2): Show | 5 | HG01074.hp2 HG02165.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1319+927_1319+930d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361176 | |||||
| chr7:74361201
|
T | TTCCTTCC others(29): Show |
1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1319+930_1319+931i others(38): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361201 | |||||
| chr7:74361205
|
T | TTCCTTCC others(17): Show |
1 | a0001c0002t0005g0079 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1319+930_1319+931i others(26): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361205 | |||||
| chr7:74361205
|
T | TTCCTTCC others(25): Show |
2 | a0001c0002t0001g0109a0001c0002t0005g0127 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1319+930_1319+931i others(34): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361205 | |||||
| chr7:74361205
|
T | TTCCTTCC others(33): Show |
1 | a0001c0002t0003g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1319+930_1319+931i others(42): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361205 | |||||
| chr7:74361205
|
T | TTCCTTCC others(41): Show |
1 | a0001c0002t0001g0190 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1319+930_1319+931i others(50): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74361205 | |||||
| chr7:74361209
|
C | T | 2 | a0001c0002t0001g0141a0001c0002t0001g0167 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1319+931C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361209 | ||||||
| chr7:74361286
|
C | T | 3 | a0001c0002t0001g0097a0001c0002t0001g0109a0001c0002t0001g0139 | 3 | HG03017.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1319+1008C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361286 | ||||||
| chr7:74361453
|
G | T | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1319+1175G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361453 | ||||||
| chr7:74361577
|
G | A | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1319+1299G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361577 | ||||||
| chr7:74361714
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1319+1436C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361714 | ||||||
| chr7:74361956
|
C | T | 7 | a0001c0002t0001g0117a0001c0002t0001g0122a0001c0002t0002g0140others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319+1678C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74361956 | ||||||
| chr7:74362031
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0154others(4): Show | 7 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319+1753G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362031 | ||||||
| chr7:74362058
|
A | G | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1319+1780A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362058 | ||||||
| chr7:74362099
|
C | CA | 21 | a0001c0001t0001g0027a0001c0001t0001g0129a0001c0001t0001g0144others(18): Show | 21 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1319+1838dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74362099 | |||||
| chr7:74362116
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1319+1838A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362116 | ||||||
| chr7:74362237
|
G | C | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1319+1959G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362237 | ||||||
| chr7:74362481
|
G | A | 1 | a0001c0001t0004g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1320-1774G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362481 | ||||||
| chr7:74362528
|
C | CT | 216 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1320-1709dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74362528 | |||||
| chr7:74362528
|
C | CTT | 20 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0033others(17): Show | 20 | HG00741.hp2 HG01884.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1320-1710_1320-170 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74362528 | |||||
| chr7:74362781
|
C | T | 5 | a0001c0001t0001g0224a0001c0002t0001g0118a0001c0002t0001g0213others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1320-1474C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362781 | ||||||
| chr7:74362845
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1320-1410G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362845 | ||||||
| chr7:74362846
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1320-1409G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362846 | ||||||
| chr7:74362919
|
C | T | 2 | a0001c0002t0001g0200a0001c0002t0001g0266 | 2 | NA18747.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1320-1336C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74362919 | ||||||
| chr7:74363580
|
G | A | 1 | a0001c0004t0002g0132 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1320-675G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74363580 | ||||||
| chr7:74363618
|
C | T | 1 | a0001c0002t0002g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1320-637C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74363618 | ||||||
| chr7:74363704
|
T | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(136): Show | 139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1320-551T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74363704 | ||||||
| chr7:74363705
|
T | C | 139 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(136): Show | 139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1320-550T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74363705 | ||||||
| chr7:74363883
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1320-372G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74363883 | ||||||
| chr7:74363895
|
C | CA | 72 | a0001c0001t0001g0092a0001c0001t0001g0125a0001c0001t0001g0137others(69): Show | 72 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1320-344dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74363895 | |||||
| chr7:74363895
|
C | CAA | 11 | a0001c0001t0001g0224a0001c0001t0002g0188a0001c0002t0001g0088others(8): Show | 11 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1320-345_1320-344d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74363895 | |||||
| chr7:74363918
|
GAGGA | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(55): Show | 58 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1320-319_1320-316d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 74363918 | |||||
| chr7:74364157
|
C | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1320-98C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74364157 | ||||||
| chr7:74364197
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1320-58G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 7/16 | chr7 | 74364197 | ||||||
| chr7:74364355
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1380+40C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74364355 | ||||||
| chr7:74364423
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1380+108G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74364423 | ||||||
| chr7:74364723
|
A | G | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1380+408A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74364723 | ||||||
| chr7:74364993
|
T | TTG | 6 | a0001c0001t0003g0056a0001c0002t0001g0186a0001c0002t0003g0065others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+735_1380+736d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
T | TTGTG | 7 | a0001c0002t0001g0164a0001c0002t0001g0205a0001c0002t0001g0223others(4): Show | 7 | HG00558.hp1 HG02145.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1380+733_1380+736d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1380+727_1380+736d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTG | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0078others(17): Show | 20 | HG00558.hp2 HG00621.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1380+735_1380+736d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTG | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0043others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(43): Show |
intron_variant | MODIFIER | c.1380+733_1380+736d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTG | T | 43 | a0001c0001t0001g0037a0001c0001t0001g0145a0001c0001t0001g0148others(40): Show | 43 | HG00609.hp1 HG00738.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1380+731_1380+736d others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(1): Show |
T | 42 | a0001c0001t0001g0076a0001c0001t0001g0144a0001c0001t0001g0150others(39): Show | 42 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1380+729_1380+736d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(3): Show |
T | 50 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(47): Show | 50 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1380+727_1380+736d others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(5): Show |
T | 14 | a0001c0001t0001g0019a0001c0001t0001g0219a0001c0001t0001g0270others(11): Show | 14 | HG01099.hp2 HG01496.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1380+725_1380+736d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(7): Show |
T | 10 | a0001c0001t0001g0113a0001c0001t0001g0138a0001c0001t0001g0155others(7): Show | 10 | HG01106.hp1 HG01258.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1380+723_1380+736d others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(9): Show |
T | 3 | a0001c0004t0012g0235a0001c0004t0012g0236a0001c0020t0006g0267 | 3 | HG00639.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1380+721_1380+736d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(11): Show |
T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+719_1380+736d others(20): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74364993
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0002t0001g0245 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1380+715_1380+736d others(24): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74364993 | |||||
| chr7:74365007
|
GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1380+693_1380+703d others(13): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365007 | ||||||
| chr7:74365497
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1182C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365497 | ||||||
| chr7:74365574
|
CG | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0189a0001c0001t0001g0191others(7): Show | 10 | HG00621.hp1 HG02056.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1380+1261delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74365574 | |||||
| chr7:74365653
|
AT | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1380+1340delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74365653 | |||||
| chr7:74365810
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1380+1495A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365810 | ||||||
| chr7:74365818
|
C | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1503C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365818 | ||||||
| chr7:74365843
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1528T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365843 | ||||||
| chr7:74365928
|
A | AT | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(10): Show | 13 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+1622dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74365928 | |||||
| chr7:74365948
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1633G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74365948 | ||||||
| chr7:74366173
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1858T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366173 | ||||||
| chr7:74366234
|
C | T | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1380+1919C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366234 | ||||||
| chr7:74366294
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+1979C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366294 | ||||||
| chr7:74366401
|
T | G | 1 | a0006c0013t0002g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1380+2086T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366401 | ||||||
| chr7:74366415
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2100A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366415 | ||||||
| chr7:74366416
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2101T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366416 | ||||||
| chr7:74366482
|
C | G | 76 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1380+2167C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366482 | ||||||
| chr7:74366513
|
A | G | 5 | a0001c0001t0001g0224a0001c0008t0009g0031a0001c0008t0009g0149others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1380+2198A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366513 | ||||||
| chr7:74366564
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1380+2249C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366564 | ||||||
| chr7:74366632
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2317C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366632 | ||||||
| chr7:74366652
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1380+2337G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366652 | ||||||
| chr7:74366667
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1380+2352A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366667 | ||||||
| chr7:74366875
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0047a0001c0001t0001g0087others(18): Show | 21 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1380+2584dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74366875 | |||||
| chr7:74366875
|
CA | C | 64 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0171others(61): Show | 64 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1380+2584delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74366875 | |||||
| chr7:74366875
|
CAA | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(13): Show | 16 | HG00323.hp2 HG01074.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1380+2583_1380+258 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74366875 | |||||
| chr7:74366875
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0201a0001c0001t0002g0030 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1380+2573_1380+258 others(16): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74366875 | |||||
| chr7:74366875
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0003g0056a0001c0001t0004g0058 | 2 | HG02683.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1380+2572_1380+258 others(17): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74366875 | |||||
| chr7:74366911
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1380+2596A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74366911 | ||||||
| chr7:74367050
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2735G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367050 | ||||||
| chr7:74367175
|
CTTTAT | C | 3 | a0001c0008t0009g0031a0001c0008t0009g0149a0001c0008t0009g0211 | 3 | HG01192.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1380+2864_1380+286 others(9): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74367175 | |||||
| chr7:74367195
|
A | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0020others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1380+2880A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367195 | ||||||
| chr7:74367227
|
G | A | 76 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1380+2912G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367227 | ||||||
| chr7:74367244
|
G | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2929G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367244 | ||||||
| chr7:74367252
|
G | A | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1380+2937G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367252 | ||||||
| chr7:74367254
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2939A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367254 | ||||||
| chr7:74367291
|
T | C | 241 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1380+2976T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367291 | ||||||
| chr7:74367381
|
G | A | 2 | a0001c0004t0002g0128a0001c0004t0002g0175 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1380+3066G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367381 | ||||||
| chr7:74367564
|
G | A | 1 | a0001c0001t0019g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1380+3249G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367564 | ||||||
| chr7:74367640
|
A | T | 5 | a0001c0001t0001g0224a0001c0008t0009g0031a0001c0008t0009g0149others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1380+3325A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367640 | ||||||
| chr7:74367673
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+3358C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367673 | ||||||
| chr7:74367721
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+3406C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367721 | ||||||
| chr7:74367769
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+3454A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367769 | ||||||
| chr7:74367772
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0154others(6): Show | 9 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1380+3457T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74367772 | ||||||
| chr7:74368020
|
T | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(138): Show | 141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1380+3705T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368020 | ||||||
| chr7:74368408
|
A | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1380+4093A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368408 | ||||||
| chr7:74368504
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1380+4189G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368504 | ||||||
| chr7:74368517
|
A | AAAAT | 6 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0002t0001g0118others(3): Show | 6 | HG01433.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380+4226_1380+422 others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74368517 | |||||
| chr7:74368526
|
A | AAAT | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+4214_1380+421 others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74368526 | |||||
| chr7:74368707
|
A | G | 1 | a0001c0002t0001g0200 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1381-4225A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368707 | ||||||
| chr7:74368735
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-4197G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368735 | ||||||
| chr7:74368844
|
C | T | 2 | a0001c0001t0001g0156a0007c0017t0004g0075 | 2 | HG01258.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1381-4088C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368844 | ||||||
| chr7:74368935
|
G | A | 5 | a0001c0001t0001g0224a0001c0008t0009g0031a0001c0008t0009g0149others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-3997G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74368935 | ||||||
| chr7:74369214
|
G | A | 2 | a0001c0001t0003g0056a0001c0001t0004g0058 | 2 | HG02683.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1381-3718G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369214 | ||||||
| chr7:74369246
|
G | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01258.hp1 HG03654.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381-3686G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369246 | ||||||
| chr7:74369283
|
G | A | 46 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(43): Show | 46 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1381-3649G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369283 | ||||||
| chr7:74369434
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-3498T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369434 | ||||||
| chr7:74369453
|
G | T | 75 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(72): Show | 75 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1381-3479G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369453 | ||||||
| chr7:74369677
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02622.hp1 HG02738.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-3255T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369677 | ||||||
| chr7:74369677
|
T | TGAAACCC others(294): Show |
1 | a0001c0001t0003g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1381-3057_1381-275 others(305): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369677 | |||||
| chr7:74369755
|
G | C | 76 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1381-3177G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369755 | ||||||
| chr7:74369758
|
G | C | 4 | a0001c0001t0002g0188a0001c0001t0003g0063a0001c0002t0001g0094others(1): Show | 4 | HG02155.hp2 NA18952.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-3174G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369758 | ||||||
| chr7:74369842
|
G | A | 36 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(33): Show | 36 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1381-3090G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369842 | ||||||
| chr7:74369854
|
C | CA | 88 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0020others(85): Show | 88 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1381-3054dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369854 | |||||
| chr7:74369854
|
C | CAA | 41 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0114others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1381-3055_1381-305 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369854 | |||||
| chr7:74369854
|
C | CAAAAAAA others(299): Show |
1 | a0001c0001t0001g0189 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1381-3054_1381-305 others(310): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369854 | |||||
| chr7:74369854
|
CAAAAAAA others(294): Show |
C | 3 | a0001c0002t0001g0218a0001c0002t0005g0169a0001c0007t0010g0048 | 3 | HG01975.hp1 HG02738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1381-3057_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369854 | |||||
| chr7:74369854
|
CAAAAAAA others(295): Show |
C | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1381-3058_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369854 | |||||
| chr7:74369855
|
AAAAAAAA others(293): Show |
A | 1 | a0001c0001t0002g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1381-3056_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369855 | |||||
| chr7:74369856
|
AAAAAAAA others(292): Show |
A | 64 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(61): Show | 64 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1381-3055_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369856 | |||||
| chr7:74369857
|
AAAAAAAA others(291): Show |
A | 12 | a0001c0001t0002g0188a0001c0001t0005g0206a0001c0001t0017g0260others(9): Show | 12 | HG01175.hp1 HG01952.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1381-3054_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369857 | |||||
| chr7:74369858
|
AAAAAAAA others(290): Show |
A | 13 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381-3006_1381-271 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369858 | |||||
| chr7:74369859
|
AAAAAAAA others(289): Show |
A | 10 | a0001c0001t0001g0138a0001c0001t0001g0155a0001c0001t0003g0062others(7): Show | 10 | HG00099.hp2 HG00673.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-3053_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369859 | |||||
| chr7:74369860
|
AAAAAAAA others(288): Show |
A | 3 | a0001c0001t0001g0150a0001c0002t0001g0226a0001c0009t0001g0126 | 3 | HG01071.hp1 HG02109.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1381-3053_1381-275 others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74369860 | |||||
| chr7:74369926
|
A | G | 4 | a0001c0002t0001g0118a0001c0002t0001g0131a0001c0002t0001g0213others(1): Show | 4 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-3006A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74369926 | ||||||
| chr7:74370026
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-2906T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370026 | ||||||
| chr7:74370045
|
C | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-2887C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370045 | ||||||
| chr7:74370051
|
G | A | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1381-2881G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370051 | ||||||
| chr7:74370143
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0196others(1): Show | 4 | HG00621.hp1 NA18945.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-2789G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370143 | ||||||
| chr7:74370155
|
C | CA | 33 | a0001c0001t0001g0037a0001c0001t0001g0076a0001c0001t0001g0085others(30): Show | 33 | HG01258.hp1 HG01884.hp1 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.1381-2757dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370155 | |||||
| chr7:74370155
|
C | CAA | 8 | a0001c0001t0001g0112a0001c0001t0001g0151a0001c0001t0001g0189others(5): Show | 8 | HG00408.hp2 HG02083.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-2758_1381-275 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370155 | |||||
| chr7:74370155
|
C | CAAAAAAA others(297): Show |
1 | a0001c0001t0001g0196 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1381-2757_1381-275 others(308): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370155 | |||||
| chr7:74370155
|
C | CAAAAAAA others(296): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1381-2757_1381-275 others(307): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370155 | |||||
| chr7:74370183
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(14): Show | 17 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381-2749A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370183 | ||||||
| chr7:74370223
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0154others(4): Show | 7 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-2709G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370223 | ||||||
| chr7:74370284
|
G | A | 1 | a0002c0006t0002g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1381-2648G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370284 | ||||||
| chr7:74370288
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-2644C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370288 | ||||||
| chr7:74370293
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0003g0064a0001c0001t0004g0066 | 3 | HG00735.hp2 HG01978.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1381-2639A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370293 | ||||||
| chr7:74370325
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1381-2607G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370325 | ||||||
| chr7:74370392
|
G | C | 76 | a0001c0001t0001g0092a0001c0001t0001g0193a0001c0001t0001g0219others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1381-2540G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370392 | ||||||
| chr7:74370455
|
C | CA | 14 | a0001c0001t0001g0123a0001c0001t0001g0189a0001c0001t0002g0152others(11): Show | 14 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1381-2461dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370455 | |||||
| chr7:74370455
|
CA | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(12): Show | 15 | HG01975.hp1 HG02257.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1381-2461delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74370455 | |||||
| chr7:74370594
|
C | A | 2 | a0001c0002t0001g0088a0001c0002t0002g0098 | 2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1381-2338C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370594 | ||||||
| chr7:74370616
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1381-2316C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370616 | ||||||
| chr7:74370696
|
A | G | 1 | a0001c0002t0001g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1381-2236A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370696 | ||||||
| chr7:74370739
|
G | A | 1 | a0001c0001t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1381-2193G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370739 | ||||||
| chr7:74370840
|
G | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(90): Show | 93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1381-2092G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370840 | ||||||
| chr7:74370959
|
G | A | 2 | a0001c0002t0001g0246a0002c0003t0002g0110 | 2 | HG02165.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1381-1973G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74370959 | ||||||
| chr7:74371209
|
G | A | 1 | a0001c0014t0003g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1381-1723G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74371209 | ||||||
| chr7:74371243
|
C | CA | 24 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 24 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1381-1666dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74371243 | |||||
| chr7:74371243
|
C | CAA | 69 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1381-1667_1381-166 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74371243 | |||||
| chr7:74371243
|
C | CAAA | 17 | a0001c0001t0001g0034a0001c0001t0005g0206a0001c0001t0017g0260others(14): Show | 17 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381-1668_1381-166 others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74371243 | |||||
| chr7:74371243
|
CA | C | 9 | a0001c0001t0001g0172a0001c0001t0003g0062a0001c0001t0006g0002others(6): Show | 9 | HG01074.hp2 HG01168.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-1666delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74371243 | |||||
| chr7:74371268
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1381-1664G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74371268 | ||||||
| chr7:74371639
|
G | C | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1381-1293G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74371639 | ||||||
| chr7:74371658
|
A | G | 2 | a0001c0002t0001g0205a0001c0002t0001g0214 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1381-1274A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74371658 | ||||||
| chr7:74371828
|
A | C | 4 | a0001c0002t0001g0088a0001c0002t0001g0197a0001c0002t0001g0250others(1): Show | 4 | NA18952.hp2 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-1104A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74371828 | ||||||
| chr7:74372181
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1381-751T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372181 | ||||||
| chr7:74372202
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1381-730G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372202 | ||||||
| chr7:74372366
|
G | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(16): Show | 19 | HG01081.hp2 HG01192.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1381-566G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372366 | ||||||
| chr7:74372400
|
CT | C | 79 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0044others(76): Show | 79 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1381-530delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74372400 | |||||
| chr7:74372401
|
T | TG | 48 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0038others(45): Show | 48 | HG00621.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1381-531_1381-530i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372401 | ||||||
| chr7:74372401
|
T | TGG | 7 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(4): Show | 7 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1381-531_1381-530i others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372401 | ||||||
| chr7:74372401
|
T | TGGG | 4 | a0001c0001t0001g0036a0001c0002t0001g0028a0001c0002t0001g0231others(1): Show | 4 | HG00642.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-531_1381-530i others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372401 | ||||||
| chr7:74372401
|
TTG | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0129a0001c0002t0001g0007others(12): Show | 15 | HG00639.hp1 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1381-530_1381-529d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372401 | ||||||
| chr7:74372402
|
T | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1381-530T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372402 | ||||||
| chr7:74372404
|
G | T | 2 | a0001c0002t0001g0159a0001c0002t0001g0255 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1381-528G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372404 | ||||||
| chr7:74372407
|
G | T | 1 | a0001c0002t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1381-525G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372407 | ||||||
| chr7:74372409
|
G | C | 2 | a0001c0001t0001g0047a0001c0018t0001g0095 | 2 | HG01081.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1381-523G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372409 | ||||||
| chr7:74372411
|
G | T | 1 | a0001c0002t0001g0186 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1381-521G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372411 | ||||||
| chr7:74372423
|
C | T | 1 | a0001c0001t0008g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1381-509C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372423 | ||||||
| chr7:74372489
|
T | A | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1381-443T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372489 | ||||||
| chr7:74372511
|
G | A | 1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1381-421G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372511 | ||||||
| chr7:74372593
|
T | TG | 69 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0044others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1381-332dupG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74372593 | |||||
| chr7:74372600
|
G | GGA | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-332_1381-331i others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372600 | ||||||
| chr7:74372644
|
C | T | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(56): Show | 59 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1381-288C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372644 | ||||||
| chr7:74372670
|
A | AC | 8 | a0001c0001t0019g0067a0001c0002t0001g0024a0001c0002t0001g0025others(5): Show | 8 | HG02109.hp2 HG03516.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-256dupC | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74372670 | |||||
| chr7:74372783
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0172 | 2 | HG01168.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1381-149G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372783 | ||||||
| chr7:74372793
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1381-139T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372793 | ||||||
| chr7:74372830
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0002t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1381-90_1381-79del others(12): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74372830 | |||||
| chr7:74372849
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1381-83T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372849 | ||||||
| chr7:74372899
|
A | AC | 18 | a0001c0001t0001g0036a0001c0001t0001g0144a0001c0001t0001g0189others(15): Show | 18 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1381-26dupC | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 74372899 | |||||
| chr7:74372901
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1381-31C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 8/16 | chr7 | 74372901 | ||||||
| chr7:74373298
|
G | A | 1 | a0001c0001t0019g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1485+262G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373298 | ||||||
| chr7:74373404
|
A | T | 1 | a0001c0002t0005g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1485+368A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373404 | ||||||
| chr7:74373419
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1485+383A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373419 | ||||||
| chr7:74373497
|
C | A | 1 | a0001c0002t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1485+461C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373497 | ||||||
| chr7:74373672
|
A | G | 2 | a0001c0007t0010g0010a0001c0007t0010g0015 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1485+636A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373672 | ||||||
| chr7:74373694
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0114 | 2 | NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1485+658T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373694 | ||||||
| chr7:74373725
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0162 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1485+689C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373725 | ||||||
| chr7:74373739
|
C | G | 1 | a0001c0002t0001g0269 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1485+703C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373739 | ||||||
| chr7:74373820
|
A | G | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+784A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373820 | ||||||
| chr7:74373897
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1485+861G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74373897 | ||||||
| chr7:74374218
|
A | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(10): Show | 13 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1485+1182A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374218 | ||||||
| chr7:74374350
|
A | G | 1 | a0001c0002t0005g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1485+1314A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374350 | ||||||
| chr7:74374581
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0224a0001c0008t0009g0031others(2): Show | 5 | HG01081.hp2 HG01192.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1306C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374581 | ||||||
| chr7:74374582
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1486-1305G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374582 | ||||||
| chr7:74374610
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1486-1277A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374610 | ||||||
| chr7:74374688
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1486-1199T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374688 | ||||||
| chr7:74374841
|
T | A | 1 | a0004c0016t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1486-1046T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74374841 | ||||||
| chr7:74375095
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1486-792T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375095 | ||||||
| chr7:74375253
|
T | TA | 3 | a0001c0008t0009g0031a0001c0008t0009g0149a0001c0008t0009g0211 | 3 | HG01192.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1486-634_1486-633i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375253 | ||||||
| chr7:74375254
|
T | A | 8 | a0001c0001t0008g0003a0001c0002t0001g0159a0001c0002t0001g0164others(5): Show | 8 | HG01192.hp1 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1486-633T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375254 | ||||||
| chr7:74375254
|
T | TA | 18 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(15): Show | 18 | HG00558.hp1 HG00673.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1486-619dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375254 | |||||
| chr7:74375254
|
TA | T | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(56): Show | 59 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1486-619delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375254 | |||||
| chr7:74375276
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1486-611C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375276 | ||||||
| chr7:74375312
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1486-575G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375312 | ||||||
| chr7:74375346
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1486-541C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375346 | ||||||
| chr7:74375400
|
A | C | 100 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(97): Show | 100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1486-487A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375400 | ||||||
| chr7:74375445
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1486-442C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375445 | ||||||
| chr7:74375512
|
C | T | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1486-375C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375512 | ||||||
| chr7:74375546
|
C | CA | 93 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0076others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1486-314dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375546 | |||||
| chr7:74375546
|
C | CAA | 29 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0193others(26): Show | 29 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1486-315_1486-314d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375546 | |||||
| chr7:74375546
|
CA | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0032others(55): Show | 58 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1486-314delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375546 | |||||
| chr7:74375837
|
T | TCCAGCCA others(1): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0202 | 3 | HG02559.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1486-39_1486-32dup others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 74375837 | |||||
| chr7:74375868
|
T | A | 1 | a0001c0001t0004g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1486-19T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 9/16 | chr7 | 74375868 | ||||||
| chr7:74376877
|
C | T | 9 | a0001c0001t0003g0055a0001c0001t0006g0002a0001c0001t0006g0014others(6): Show | 9 | HG01074.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2421+55C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74376877 | ||||||
| chr7:74376926
|
C | G | 1 | a0001c0002t0001g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2421+104C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74376926 | ||||||
| chr7:74376927
|
G | A | 57 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(54): Show | 57 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.2421+105G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74376927 | ||||||
| chr7:74377359
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2421+537C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377359 | ||||||
| chr7:74377499
|
C | T | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2421+677C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377499 | ||||||
| chr7:74377702
|
T | C | 1 | a0001c0002t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2421+880T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377702 | ||||||
| chr7:74377811
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2421+989C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377811 | ||||||
| chr7:74377828
|
A | AT | 15 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0202others(12): Show | 15 | HG00323.hp2 HG01106.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.2421+1020dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 74377828 | |||||
| chr7:74377844
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2421+1022A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377844 | ||||||
| chr7:74377954
|
T | C | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2421+1132T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74377954 | ||||||
| chr7:74378106
|
G | A | 11 | a0001c0001t0003g0056a0001c0001t0003g0070a0001c0002t0001g0117others(8): Show | 11 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2421+1284G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378106 | ||||||
| chr7:74378134
|
G | T | 1 | a0001c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2421+1312G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378134 | ||||||
| chr7:74378177
|
G | T | 2 | a0001c0001t0002g0012a0001c0002t0002g0257 | 2 | HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2421+1355G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378177 | ||||||
| chr7:74378264
|
A | G | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2421+1442A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378264 | ||||||
| chr7:74378318
|
G | A | 2 | a0001c0002t0001g0205a0001c0002t0001g0214 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2421+1496G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378318 | ||||||
| chr7:74378374
|
C | G | 1 | a0001c0002t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2421+1552C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378374 | ||||||
| chr7:74378375
|
G | A | 9 | a0001c0001t0003g0055a0001c0001t0006g0002a0001c0001t0006g0014others(6): Show | 9 | HG01074.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2421+1553G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378375 | ||||||
| chr7:74378450
|
G | T | 1 | a0001c0002t0001g0181 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2421+1628G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378450 | ||||||
| chr7:74378457
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2421+1635G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378457 | ||||||
| chr7:74378583
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2421+1761A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378583 | ||||||
| chr7:74378601
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0162a0001c0001t0001g0224 | 3 | HG03130.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2421+1779A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74378601 | ||||||
| chr7:74379329
|
G | GA | 26 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(23): Show | 26 | HG00438.hp1 HG01081.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.2422-1463dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 74379329 | |||||
| chr7:74379492
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2422-1314G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74379492 | ||||||
| chr7:74379678
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2422-1128C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74379678 | ||||||
| chr7:74379778
|
TAAAA | T | 3 | a0002c0003t0002g0183a0002c0003t0004g0054a0002c0003t0004g0074 | 3 | NA18960.hp2 NA18984.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2422-1024_2422-102 others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 74379778 | |||||
| chr7:74379944
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(11): Show | 14 | HG01081.hp2 HG02257.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422-862C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74379944 | ||||||
| chr7:74380224
|
G | C | 2 | a0001c0001t0001g0178a0001c0002t0001g0217 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2422-582G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380224 | ||||||
| chr7:74380291
|
G | C | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2422-515G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380291 | ||||||
| chr7:74380513
|
T | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0001g0124others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2422-293T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380513 | ||||||
| chr7:74380565
|
G | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2422-241G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380565 | ||||||
| chr7:74380646
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2422-160G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380646 | ||||||
| chr7:74380665
|
G | A | 1 | a0002c0006t0002g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2422-141G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380665 | ||||||
| chr7:74380684
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2422-122G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380684 | ||||||
| chr7:74380719
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2422-87C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380719 | ||||||
| chr7:74380731
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2422-75G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380731 | ||||||
| chr7:74380783
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2422-23C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 10/16 | chr7 | 74380783 | ||||||
| chr7:74381101
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2479+238G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381101 | ||||||
| chr7:74381244
|
A | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2479+381A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381244 | ||||||
| chr7:74381401
|
G | C | 1 | a0002c0003t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2479+538G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381401 | ||||||
| chr7:74381423
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2479+560G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381423 | ||||||
| chr7:74381433
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0172 | 2 | HG01168.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2479+570C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381433 | ||||||
| chr7:74381478
|
T | C | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2479+615T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381478 | ||||||
| chr7:74381583
|
C | T | 1 | a0001c0002t0001g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2479+720C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381583 | ||||||
| chr7:74381991
|
G | T | 1 | a0001c0019t0007g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2479+1128G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74381991 | ||||||
| chr7:74382009
|
T | C | 5 | a0001c0001t0001g0178a0001c0002t0001g0217a0001c0008t0009g0031others(2): Show | 5 | HG01192.hp1 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2479+1146T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74382009 | ||||||
| chr7:74382090
|
A | AT | 146 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.2479+1237dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74382090 | |||||
| chr7:74382290
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2479+1427A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74382290 | ||||||
| chr7:74382291
|
T | C | 1 | a0001c0002t0001g0269 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2479+1428T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74382291 | ||||||
| chr7:74382304
|
C | CT | 140 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2479+1459dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74382304 | |||||
| chr7:74382336
|
A | C | 4 | a0001c0002t0001g0118a0001c0002t0001g0131a0001c0002t0001g0213others(1): Show | 4 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2479+1473A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74382336 | ||||||
| chr7:74382471
|
A | AT | 27 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0032others(24): Show | 27 | HG00621.hp1 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.2479+1630dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74382471 | |||||
| chr7:74382471
|
AT | A | 8 | a0001c0001t0001g0268a0001c0001t0002g0221a0001c0002t0001g0207others(5): Show | 8 | HG01070.hp2 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2479+1630delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74382471 | |||||
| chr7:74382605
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2479+1742C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74382605 | ||||||
| chr7:74383063
|
G | C | 1 | a0001c0002t0001g0096 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2479+2200G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383063 | ||||||
| chr7:74383080
|
C | CA | 26 | a0001c0001t0001g0020a0001c0001t0001g0104a0001c0001t0001g0137others(23): Show | 26 | HG00741.hp1 HG00741.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.2479+2238dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74383080 | |||||
| chr7:74383080
|
CA | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(13): Show | 16 | HG01074.hp2 HG01884.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2479+2238delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74383080 | |||||
| chr7:74383147
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(8): Show | 11 | HG01243.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2479+2284G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383147 | ||||||
| chr7:74383635
|
C | T | 23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0104others(20): Show | 23 | HG00639.hp1 HG00673.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2479+2772C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383635 | ||||||
| chr7:74383697
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2480-2824G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383697 | ||||||
| chr7:74383907
|
C | G | 92 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2480-2614C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383907 | ||||||
| chr7:74383949
|
T | C | 48 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0129others(45): Show | 48 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2480-2572T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383949 | ||||||
| chr7:74383975
|
T | C | 1 | a0001c0001t0008g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2480-2546T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74383975 | ||||||
| chr7:74384050
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2480-2471G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384050 | ||||||
| chr7:74384061
|
C | T | 4 | a0001c0002t0001g0199a0001c0002t0016g0230a0001c0004t0002g0132others(1): Show | 4 | HG00408.hp1 HG00438.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2480-2460C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384061 | ||||||
| chr7:74384115
|
G | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(58): Show | 61 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2480-2406G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384115 | ||||||
| chr7:74384145
|
G | A | 8 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2480-2376G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384145 | ||||||
| chr7:74384146
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2480-2375C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384146 | ||||||
| chr7:74384275
|
C | T | 99 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(96): Show | 99 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2480-2246C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384275 | ||||||
| chr7:74384441
|
A | AT | 103 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0047others(100): Show | 103 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.2480-2058dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74384441 | |||||
| chr7:74384441
|
A | ATT | 20 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(17): Show | 20 | HG00735.hp2 HG02083.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2480-2059_2480-205 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74384441 | |||||
| chr7:74384482
|
G | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2480-2039G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384482 | ||||||
| chr7:74384506
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.2480-2015T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384506 | ||||||
| chr7:74384532
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2480-1989G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384532 | ||||||
| chr7:74384683
|
C | T | 2 | a0001c0004t0012g0235a0001c0004t0012g0236 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2480-1838C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384683 | ||||||
| chr7:74384725
|
C | T | 1 | a0001c0001t0007g0147 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2480-1796C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74384725 | ||||||
| chr7:74385003
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2480-1518G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385003 | ||||||
| chr7:74385043
|
G | A | 2 | a0001c0001t0003g0055a0001c0002t0001g0141 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2480-1478G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385043 | ||||||
| chr7:74385113
|
T | C | 103 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 103 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.2480-1408T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385113 | ||||||
| chr7:74385122
|
C | CA | 52 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0047others(49): Show | 52 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.2480-1377dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385122 | |||||
| chr7:74385122
|
CA | C | 6 | a0001c0001t0008g0003a0001c0002t0001g0213a0001c0002t0001g0237others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2480-1377delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385122 | |||||
| chr7:74385252
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(66): Show | 69 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2480-1269G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385252 | ||||||
| chr7:74385322
|
C | T | 44 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0129others(41): Show | 44 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2480-1199C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385322 | ||||||
| chr7:74385464
|
C | CA | 12 | a0001c0001t0001g0020a0001c0001t0001g0144a0001c0001t0002g0093others(9): Show | 12 | HG00609.hp1 HG00741.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2480-1039dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385464 | |||||
| chr7:74385464
|
CA | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0172a0001c0001t0002g0030others(3): Show | 6 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2480-1039delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385464 | |||||
| chr7:74385511
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2480-1010G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385511 | ||||||
| chr7:74385621
|
A | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(216): Show | 219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.2480-900A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385621 | ||||||
| chr7:74385737
|
C | CT | 18 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0137others(15): Show | 18 | HG00741.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2480-762dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385737 | |||||
| chr7:74385737
|
CTTT | C | 10 | a0001c0001t0001g0034a0001c0001t0001g0104a0001c0001t0001g0191others(7): Show | 10 | HG00621.hp1 HG02056.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2480-764_2480-762d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385737 | |||||
| chr7:74385737
|
CTTTT | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.2480-765_2480-762d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74385737 | |||||
| chr7:74385801
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2480-720G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385801 | ||||||
| chr7:74385820
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2480-701G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385820 | ||||||
| chr7:74385970
|
G | A | 3 | a0001c0002t0001g0122a0002c0003t0002g0049a0002c0003t0002g0050 | 3 | HG01243.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2480-551G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74385970 | ||||||
| chr7:74386043
|
C | CT | 47 | a0001c0001t0001g0020a0001c0001t0001g0076a0001c0001t0001g0085others(44): Show | 47 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.2480-462dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 74386043 | |||||
| chr7:74386071
|
C | T | 8 | a0001c0001t0002g0111a0001c0001t0002g0130a0001c0001t0002g0184others(5): Show | 8 | HG00741.hp1 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2480-450C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386071 | ||||||
| chr7:74386086
|
C | T | 4 | a0001c0001t0001g0047a0001c0002t0001g0122a0002c0003t0002g0049others(1): Show | 4 | HG01081.hp2 HG01243.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2480-435C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386086 | ||||||
| chr7:74386110
|
C | T | 7 | a0001c0001t0001g0178a0001c0001t0003g0055a0001c0002t0001g0141others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2480-411C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386110 | ||||||
| chr7:74386143
|
G | A | 2 | a0001c0009t0001g0082a0001c0009t0001g0126 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2480-378G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386143 | ||||||
| chr7:74386231
|
A | G | 2 | a0001c0004t0012g0235a0001c0004t0012g0236 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2480-290A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386231 | ||||||
| chr7:74386381
|
C | T | 75 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0092others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2480-140C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 11/16 | chr7 | 74386381 | ||||||
| chr7:74386689
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(66): Show | 69 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2563+85A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74386689 | ||||||
| chr7:74386715
|
G | A | 2 | a0001c0001t0003g0055a0001c0002t0001g0141 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2563+111G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74386715 | ||||||
| chr7:74386788
|
C | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0134a0001c0002t0002g0119 | 3 | HG00558.hp2 NA18940.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2563+184C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74386788 | ||||||
| chr7:74386924
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(66): Show | 69 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2563+320G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74386924 | ||||||
| chr7:74386980
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2563+376G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74386980 | ||||||
| chr7:74387022
|
CA | C | 39 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0086others(36): Show | 39 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2563+438delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 74387022 | |||||
| chr7:74387022
|
CAA | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2563+437_2563+438d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 74387022 | |||||
| chr7:74387054
|
A | G | 3 | a0001c0002t0001g0122a0002c0003t0002g0049a0002c0003t0002g0050 | 3 | HG01243.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2563+450A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387054 | ||||||
| chr7:74387238
|
T | G | 9 | a0001c0001t0001g0187a0001c0002t0001g0090a0001c0002t0001g0096others(6): Show | 9 | HG00609.hp1 HG00738.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.2563+634T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387238 | ||||||
| chr7:74387341
|
C | T | 2 | a0001c0001t0003g0055a0001c0002t0001g0141 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2563+737C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387341 | ||||||
| chr7:74387547
|
G | A | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2563+943G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387547 | ||||||
| chr7:74387615
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2563+1011G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387615 | ||||||
| chr7:74387809
|
G | T | 3 | a0001c0002t0001g0122a0002c0003t0002g0049a0002c0003t0002g0050 | 3 | HG01243.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2563+1205G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387809 | ||||||
| chr7:74387829
|
C | T | 11 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(8): Show | 11 | HG01433.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2563+1225C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387829 | ||||||
| chr7:74387968
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2564-1135G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74387968 | ||||||
| chr7:74388045
|
C | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2564-1058C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388045 | ||||||
| chr7:74388101
|
G | A | 3 | a0001c0002t0001g0122a0002c0003t0002g0049a0002c0003t0002g0050 | 3 | HG01243.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2564-1002G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388101 | ||||||
| chr7:74388229
|
G | C | 1 | a0001c0001t0002g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2564-874G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388229 | ||||||
| chr7:74388340
|
C | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(28): Show | 31 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2564-763C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388340 | ||||||
| chr7:74388340
|
C | CA | 3 | a0001c0002t0001g0099a0001c0002t0001g0102a0001c0014t0003g0060 | 3 | HG03669.hp1 HG03927.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2564-762dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 74388340 | |||||
| chr7:74388342
|
C | A | 214 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(211): Show | 214 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.2564-761C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388342 | ||||||
| chr7:74388694
|
T | C | 3 | a0001c0007t0010g0010a0001c0007t0010g0015a0001c0007t0010g0048 | 3 | HG02280.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2564-409T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388694 | ||||||
| chr7:74388727
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2564-376G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388727 | ||||||
| chr7:74388795
|
C | CA | 25 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0036others(22): Show | 25 | HG00621.hp1 HG01928.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.2564-296dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 74388795 | |||||
| chr7:74388956
|
T | TA | 8 | a0001c0001t0001g0233a0001c0001t0002g0133a0001c0001t0003g0063others(5): Show | 8 | HG00438.hp1 HG00621.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.2564-140dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 74388956 | |||||
| chr7:74388966
|
G | A | 2 | a0002c0003t0002g0049a0002c0003t0002g0050 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2564-137G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388966 | ||||||
| chr7:74388973
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2564-130C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74388973 | ||||||
| chr7:74389016
|
C | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2564-87C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 12/16 | chr7 | 74389016 | ||||||
| chr7:74389267
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | splice_region_variant&intron_variant | LOW | c.2720+8G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74389267 | ||||||
| chr7:74389314
|
T | A | 155 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2720+55T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74389314 | ||||||
| chr7:74389588
|
T | TA | 89 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0052others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.2720+354dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74389588 | |||||
| chr7:74389588
|
T | TAA | 14 | a0001c0001t0001g0178a0001c0001t0003g0073a0001c0001t0008g0029others(11): Show | 14 | HG01175.hp1 HG01192.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2720+353_2720+354d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74389588 | |||||
| chr7:74389588
|
TA | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(8): Show | 11 | HG01070.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2720+354delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74389588 | |||||
| chr7:74389588
|
TAAAAAAA others(5): Show |
T | 31 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(28): Show | 31 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2720+343_2720+354d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74389588 | |||||
| chr7:74389674
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2720+415G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74389674 | ||||||
| chr7:74389920
|
GT | G | 156 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2720+673delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74389920 | |||||
| chr7:74389962
|
A | G | 11 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0025others(8): Show | 11 | HG01433.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2720+703A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74389962 | ||||||
| chr7:74390115
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2720+856G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390115 | ||||||
| chr7:74390122
|
A | AAG | 5 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0123others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2720+877_2720+878d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390122 | |||||
| chr7:74390134
|
G | GAGAGAA | 37 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0076others(34): Show | 37 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.2720+878_2720+879i others(8): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390134 | |||||
| chr7:74390136
|
G | GAGAAAGA others(13): Show |
4 | a0001c0001t0001g0180a0001c0001t0001g0201a0001c0001t0002g0030others(1): Show | 4 | HG02165.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+878_2720+879i others(22): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390136 | |||||
| chr7:74390136
|
GAA | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0006g0002others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+879_2720+880d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390136 | |||||
| chr7:74390138
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2720+879A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390138 | ||||||
| chr7:74390148
|
GAA | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0004g0058others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.2720+893_2720+894d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390148 | |||||
| chr7:74390150
|
AAAAGAAA others(12): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2720+906_2720+924d others(21): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390150 | |||||
| chr7:74390152
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0007g0146others(1): Show | 4 | HG01884.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+893A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390152 | ||||||
| chr7:74390154
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0007g0146others(1): Show | 4 | HG01884.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+895G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390154 | ||||||
| chr7:74390161
|
AG | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0006g0002others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+903delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390161 | ||||||
| chr7:74390162
|
G | GA | 3 | a0001c0001t0001g0180a0001c0001t0001g0201a0001c0001t0002g0030 | 3 | HG02818.hp2 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2720+905dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAA | 18 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0145others(15): Show | 18 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2720+905_2720+906i others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAAAAGA | 9 | a0001c0001t0001g0052a0001c0001t0001g0125a0001c0001t0003g0055others(6): Show | 9 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2720+905_2720+906i others(9): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAAAAGA others(4): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0148a0001c0002t0001g0167others(2): Show | 5 | HG00609.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2720+905_2720+906i others(13): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAAAAGA others(12): Show |
1 | a0001c0002t0001g0121 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2720+905_2720+906i others(21): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAAAAGA others(20): Show |
1 | a0001c0001t0001g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2720+905_2720+906i others(29): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAGA | 19 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0120others(16): Show | 19 | HG00621.hp1 HG00741.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2720+963_2720+966d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAGAAAG others(1): Show |
9 | a0001c0001t0001g0085a0001c0001t0001g0162a0001c0001t0001g0193others(6): Show | 9 | HG01943.hp1 HG02132.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2720+959_2720+966d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
G | GAAGAAAG others(5): Show |
2 | a0001c0001t0001g0189a0002c0003t0002g0177 | 2 | HG02630.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2720+955_2720+966d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGA | G | 22 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0113others(19): Show | 22 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2720+963_2720+966d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGAAAG others(1): Show |
G | 23 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(20): Show | 23 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2720+959_2720+966d others(10): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGAAAG others(5): Show |
G | 13 | a0001c0001t0001g0112a0001c0001t0002g0051a0001c0001t0014g0198others(10): Show | 13 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2720+955_2720+966d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGAAAG others(9): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2720+951_2720+966d others(18): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGAAAG others(13): Show |
G | 2 | a0001c0001t0001g0172a0001c0001t0001g0208 | 2 | HG01123.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2720+947_2720+966d others(22): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390162
|
GAAGAAAG others(17): Show |
G | 1 | a0007c0017t0004g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2720+943_2720+966d others(26): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390162 | |||||
| chr7:74390164
|
AG | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0123others(10): Show | 13 | HG01884.hp1 HG01975.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2720+906delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAG | A | 8 | a0001c0001t0003g0073a0001c0002t0001g0102a0001c0002t0001g0209others(5): Show | 8 | HG00323.hp2 HG01071.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2720+906_2720+910d others(7): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(2): Show |
A | 33 | a0001c0001t0001g0021a0001c0001t0001g0108a0001c0001t0001g0220others(30): Show | 33 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2720+906_2720+914d others(11): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(6): Show |
A | 17 | a0001c0001t0001g0037a0001c0001t0001g0219a0001c0001t0001g0274others(14): Show | 17 | HG00408.hp1 HG01081.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.2720+906_2720+918d others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(10): Show |
A | 2 | a0001c0002t0001g0091a0001c0007t0007g0013 | 2 | HG02717.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2720+906_2720+922d others(19): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(18): Show |
A | 2 | a0001c0001t0002g0134a0001c0002t0002g0158 | 2 | NA18971.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2720+906_2720+930d others(27): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(22): Show |
A | 24 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(21): Show | 24 | HG00558.hp2 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.2720+906_2720+934d others(31): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390164
|
AGAAAGAA others(26): Show |
A | 2 | a0001c0001t0003g0064a0004c0016t0001g0212 | 2 | HG00735.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2720+906_2720+938d others(35): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390164 | ||||||
| chr7:74390165
|
G | A | 2 | a0001c0001t0001g0092a0001c0002t0002g0243 | 2 | HG01175.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2720+906G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390165 | ||||||
| chr7:74390167
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0007g0146others(1): Show | 4 | HG01884.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+908A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390167 | ||||||
| chr7:74390169
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0007g0146others(1): Show | 4 | HG01884.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+910G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390169 | ||||||
| chr7:74390217
|
GAAAGAAA others(5): Show |
G | 1 | a0001c0002t0001g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2720+961_2720+972d others(14): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390217 | |||||
| chr7:74390222
|
A | G | 2 | a0001c0002t0001g0181a0001c0020t0006g0267 | 2 | HG00639.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2720+963A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390222 | ||||||
| chr7:74390224
|
A | T | 2 | a0001c0001t0001g0274a0005c0012t0001g0265 | 2 | HG01928.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2720+965A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390224 | ||||||
| chr7:74390225
|
GGATT | G | 7 | a0001c0001t0001g0092a0001c0001t0008g0029a0001c0002t0001g0185others(4): Show | 7 | HG00642.hp1 HG00733.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2720+967_2720+970d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390225 | ||||||
| chr7:74390226
|
G | A | 93 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.2720+967G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390226 | ||||||
| chr7:74390228
|
T | A | 4 | a0001c0002t0001g0121a0001c0002t0001g0210a0001c0002t0001g0245others(1): Show | 4 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+969T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390228 | ||||||
| chr7:74390229
|
T | G | 4 | a0001c0002t0001g0121a0001c0002t0001g0210a0001c0002t0001g0245others(1): Show | 4 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+970T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390229 | ||||||
| chr7:74390647
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2720+1388G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390647 | ||||||
| chr7:74390743
|
C | CGG | 12 | a0001c0001t0001g0019a0001c0001t0001g0078a0001c0001t0001g0180others(9): Show | 12 | HG00140.hp1 HG01952.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.2720+1487_2720+148 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390743 | |||||
| chr7:74390743
|
C | T | 5 | a0001c0002t0001g0007a0001c0002t0001g0041a0002c0006t0002g0023others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2720+1484C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390743 | ||||||
| chr7:74390746
|
GGT | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2720+1489_2720+149 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74390746 | |||||
| chr7:74390747
|
GT | G | 71 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0092others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2720+1489delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390747 | ||||||
| chr7:74390748
|
T | G | 43 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0076others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.2720+1489T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390748 | ||||||
| chr7:74390749
|
G | GT | 36 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0076others(33): Show | 36 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2720+1490_2720+149 others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390749 | ||||||
| chr7:74390750
|
G | T | 1 | a0001c0002t0002g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2720+1491G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390750 | ||||||
| chr7:74390751
|
G | T | 102 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(99): Show | 102 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2720+1492G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390751 | ||||||
| chr7:74390855
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2720+1596C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390855 | ||||||
| chr7:74390869
|
G | A | 1 | a0001c0001t0008g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2720+1610G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390869 | ||||||
| chr7:74390942
|
G | A | 3 | a0001c0002t0003g0065a0001c0009t0001g0082a0001c0009t0001g0126 | 3 | HG01070.hp2 HG01071.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2720+1683G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74390942 | ||||||
| chr7:74391032
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2720+1773A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391032 | ||||||
| chr7:74391047
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2720+1788C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391047 | ||||||
| chr7:74391184
|
T | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(25): Show | 28 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2720+1925T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391184 | ||||||
| chr7:74391204
|
G | C | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2720+1945G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391204 | ||||||
| chr7:74391205
|
G | C | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2720+1946G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391205 | ||||||
| chr7:74391492
|
C | T | 1 | a0008c0021t0001g0136 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2720+2233C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391492 | ||||||
| chr7:74391516
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2720+2257A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391516 | ||||||
| chr7:74391587
|
A | C | 217 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(214): Show | 217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2720+2328A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391587 | ||||||
| chr7:74391649
|
G | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(24): Show | 27 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2720+2390G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391649 | ||||||
| chr7:74391835
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2720+2576A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74391835 | ||||||
| chr7:74392068
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2720+2809G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74392068 | ||||||
| chr7:74392099
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG02622.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2720+2840C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74392099 | ||||||
| chr7:74392327
|
G | T | 1 | a0001c0002t0002g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2720+3068G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74392327 | ||||||
| chr7:74392350
|
CA | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.2720+3105delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74392350 | |||||
| chr7:74392360
|
AAAAAGAA others(4): Show |
A | 1 | a0001c0001t0002g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2720+3105_2720+311 others(15): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74392360 | |||||
| chr7:74392371
|
G | A | 1 | a0001c0002t0005g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2720+3112G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74392371 | ||||||
| chr7:74392869
|
A | T | 2 | a0001c0001t0001g0156a0001c0002t0002g0238 | 2 | NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2720+3610A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74392869 | ||||||
| chr7:74393034
|
C | CT | 14 | a0001c0001t0001g0037a0001c0001t0001g0151a0001c0001t0001g0189others(11): Show | 14 | HG00609.hp1 HG01978.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2720+3794dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74393034 | |||||
| chr7:74393034
|
CT | C | 67 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0092others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2720+3794delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74393034 | |||||
| chr7:74393070
|
C | T | 2 | a0001c0001t0003g0055a0001c0002t0001g0141 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2720+3811C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393070 | ||||||
| chr7:74393097
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0002g0030 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2720+3838G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393097 | ||||||
| chr7:74393301
|
T | C | 1 | a0001c0002t0001g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2721-3773T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393301 | ||||||
| chr7:74393631
|
G | A | 1 | a0001c0020t0006g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2721-3443G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393631 | ||||||
| chr7:74393901
|
A | C | 142 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 142 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.2721-3173A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393901 | ||||||
| chr7:74393966
|
A | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.2721-3108A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393966 | ||||||
| chr7:74393989
|
T | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.2721-3085T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74393989 | ||||||
| chr7:74394243
|
T | TTC | 5 | a0001c0001t0001g0154a0001c0001t0001g0270a0001c0001t0004g0058others(2): Show | 5 | HG00639.hp1 HG00673.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-2830_2721-282 others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74394243 | |||||
| chr7:74394244
|
T | TC | 102 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(99): Show | 102 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.2721-2830_2721-282 others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394244 | ||||||
| chr7:74394245
|
A | AT | 19 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0171others(16): Show | 19 | HG00621.hp2 HG00735.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2721-2807dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74394245 | |||||
| chr7:74394245
|
A | C | 5 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0002g0046others(2): Show | 5 | HG03130.hp2 NA18951.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-2829A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394245 | ||||||
| chr7:74394245
|
A | T | 107 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(104): Show | 107 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.2721-2829A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394245 | ||||||
| chr7:74394245
|
AT | A | 5 | a0001c0001t0005g0206a0001c0001t0006g0002a0001c0001t0006g0016others(2): Show | 5 | HG01074.hp2 HG02055.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-2807delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74394245 | |||||
| chr7:74394582
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2721-2492T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394582 | ||||||
| chr7:74394821
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2721-2253G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394821 | ||||||
| chr7:74394973
|
T | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.2721-2101T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74394973 | ||||||
| chr7:74395063
|
C | T | 2 | a0001c0002t0001g0226a0001c0002t0001g0234 | 2 | NA18951.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2721-2011C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395063 | ||||||
| chr7:74395124
|
T | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.2721-1950T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395124 | ||||||
| chr7:74395183
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2721-1891G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395183 | ||||||
| chr7:74395183
|
G | C | 1 | a0001c0002t0001g0226 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2721-1891G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395183 | ||||||
| chr7:74395236
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2721-1838C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395236 | ||||||
| chr7:74395365
|
A | G | 1 | a0002c0003t0002g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2721-1709A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395365 | ||||||
| chr7:74395522
|
C | T | 2 | a0001c0001t0001g0092a0001c0002t0002g0232 | 2 | HG02523.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2721-1552C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395522 | ||||||
| chr7:74395766
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.2721-1308A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395766 | ||||||
| chr7:74395824
|
T | C | 68 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0092others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2721-1250T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395824 | ||||||
| chr7:74395841
|
GT | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(45): Show | 48 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.2721-1232delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395841 | ||||||
| chr7:74395843
|
A | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0034others(45): Show | 48 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.2721-1231A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395843 | ||||||
| chr7:74395907
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 138 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.2721-1167C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74395907 | ||||||
| chr7:74396078
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2721-996C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396078 | ||||||
| chr7:74396295
|
C | T | 2 | a0001c0004t0012g0235a0001c0004t0012g0236 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2721-779C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396295 | ||||||
| chr7:74396333
|
G | A | 91 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(88): Show | 91 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.2721-741G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396333 | ||||||
| chr7:74396375
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2721-699G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396375 | ||||||
| chr7:74396404
|
A | T | 1 | a0001c0002t0001g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2721-670A>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396404 | ||||||
| chr7:74396460
|
ATG | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0053others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.2721-594_2721-593d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74396460 | |||||
| chr7:74396460
|
ATGTG | A | 108 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0047others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2721-596_2721-593d others(6): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 74396460 | |||||
| chr7:74396709
|
T | C | 1 | a0001c0001t0008g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2721-365T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396709 | ||||||
| chr7:74396776
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2721-298C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396776 | ||||||
| chr7:74396816
|
C | T | 196 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 196 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.2721-258C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396816 | ||||||
| chr7:74396949
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0137a0001c0002t0001g0205others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-125T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 13/16 | chr7 | 74396949 | ||||||
| chr7:74397317
|
G | A | 1 | a0001c0002t0001g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2880+84G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397317 | ||||||
| chr7:74397543
|
C | A | 6 | a0001c0001t0001g0047a0001c0007t0007g0004a0001c0007t0007g0013others(3): Show | 6 | HG01081.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2880+310C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397543 | ||||||
| chr7:74397657
|
G | GT | 9 | a0001c0001t0001g0137a0001c0001t0001g0219a0001c0001t0001g0220others(6): Show | 9 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2880+432dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74397657 | |||||
| chr7:74397658
|
T | G | 1 | a0002c0015t0002g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2880+425T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397658 | ||||||
| chr7:74397660
|
T | G | 4 | a0001c0001t0006g0002a0001c0001t0006g0014a0001c0001t0006g0016others(1): Show | 4 | HG01074.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2880+427T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397660 | ||||||
| chr7:74397665
|
TG | T | 116 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0019others(113): Show | 116 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2880+433delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397665 | ||||||
| chr7:74397666
|
G | GT | 15 | a0001c0001t0002g0006a0001c0001t0002g0194a0001c0001t0002g0259others(12): Show | 15 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.2880+451dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74397666 | |||||
| chr7:74397666
|
G | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0034others(76): Show | 79 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.2880+433G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397666 | ||||||
| chr7:74397670
|
T | G | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2880+437T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397670 | ||||||
| chr7:74397728
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2880+495G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397728 | ||||||
| chr7:74397767
|
C | T | 5 | a0002c0003t0002g0177a0002c0006t0002g0023a0002c0006t0002g0040others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2880+534C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397767 | ||||||
| chr7:74397815
|
C | T | 2 | a0001c0007t0010g0010a0001c0007t0010g0015 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2880+582C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397815 | ||||||
| chr7:74397827
|
T | C | 200 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2880+594T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397827 | ||||||
| chr7:74397860
|
G | C | 1 | a0001c0002t0001g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2880+627G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397860 | ||||||
| chr7:74397945
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0014a0001c0001t0006g0016others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2880+712G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397945 | ||||||
| chr7:74397963
|
G | A | 181 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.2880+730G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74397963 | ||||||
| chr7:74398316
|
G | A | 1 | a0001c0002t0003g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2880+1083G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398316 | ||||||
| chr7:74398439
|
G | C | 9 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2880+1206G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398439 | ||||||
| chr7:74398456
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2880+1223G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398456 | ||||||
| chr7:74398616
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0014a0001c0001t0006g0016others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2880+1383G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398616 | ||||||
| chr7:74398627
|
A | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2880+1394A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398627 | ||||||
| chr7:74398772
|
G | GT | 199 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2880+1541dupT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74398772 | |||||
| chr7:74398835
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2881-1535C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398835 | ||||||
| chr7:74398950
|
G | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2881-1420G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74398950 | ||||||
| chr7:74399039
|
TA | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0014a0001c0001t0006g0016others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2881-1330delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399039 | ||||||
| chr7:74399107
|
C | CTGGGCAG others(17): Show |
181 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.2881-1260_2881-123 others(28): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74399107 | |||||
| chr7:74399416
|
C | T | 13 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(10): Show | 13 | HG01081.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2881-954C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399416 | ||||||
| chr7:74399439
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2881-931G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399439 | ||||||
| chr7:74399542
|
T | TG | 58 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2881-815dupG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74399542 | |||||
| chr7:74399542
|
T | TGG | 35 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0001g0108others(32): Show | 35 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2881-816_2881-815d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74399542 | |||||
| chr7:74399542
|
TG | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(50): Show | 53 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.2881-815delG | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74399542 | |||||
| chr7:74399542
|
TGG | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0148others(21): Show | 24 | HG00738.hp1 HG01071.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2881-816_2881-815d others(4): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74399542 | |||||
| chr7:74399543
|
G | GC | 4 | a0002c0003t0002g0080a0002c0003t0002g0183a0002c0003t0004g0054others(1): Show | 4 | HG00438.hp2 NA18960.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-827_2881-826i others(3): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399543 | ||||||
| chr7:74399543
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-827G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399543 | ||||||
| chr7:74399544
|
G | C | 4 | a0002c0003t0002g0110a0002c0003t0002g0160a0002c0003t0004g0072others(1): Show | 4 | HG01975.hp2 HG02015.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-826G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399544 | ||||||
| chr7:74399544
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2881-826G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399544 | ||||||
| chr7:74399550
|
G | C | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-820G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399550 | ||||||
| chr7:74399552
|
G | T | 1 | a0001c0002t0002g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2881-818G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399552 | ||||||
| chr7:74399556
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2881-814T>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399556 | ||||||
| chr7:74399633
|
G | A | 1 | a0001c0001t0008g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2881-737G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399633 | ||||||
| chr7:74399796
|
T | C | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2881-574T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399796 | ||||||
| chr7:74399805
|
G | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 69 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.2881-565G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399805 | ||||||
| chr7:74399816
|
A | G | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-554A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399816 | ||||||
| chr7:74399832
|
G | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-538G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74399832 | ||||||
| chr7:74400027
|
C | T | 9 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2881-343C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | chr7 | 74400027 | ||||||
| chr7:74400149
|
C | CA | 15 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0148others(12): Show | 15 | HG00642.hp1 HG00741.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2881-200dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74400149 | |||||
| chr7:74400149
|
C | CAAA | 6 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(3): Show | 6 | HG01081.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2881-202_2881-200d others(5): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74400149 | |||||
| chr7:74400149
|
CA | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0202others(4): Show | 7 | HG00733.hp2 HG02155.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2881-200delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 74400149 | |||||
| chr7:74400699
|
G | A | 2 | a0001c0007t0010g0010a0001c0007t0010g0015 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3066+144G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74400699 | ||||||
| chr7:74400842
|
C | G | 1 | a0001c0002t0001g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3066+287C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74400842 | ||||||
| chr7:74400923
|
G | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0002t0001g0167 | 3 | HG02717.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3066+368G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74400923 | ||||||
| chr7:74400926
|
G | A | 5 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0118others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+371G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74400926 | ||||||
| chr7:74400935
|
C | G | 1 | a0001c0007t0010g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3066+380C>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74400935 | ||||||
| chr7:74400986
|
T | TTGATCTG others(214): Show |
1 | a0001c0007t0007g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3066+438_3067-292d others(223): Show |
CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr7 | 74400986 | |||||
| chr7:74401089
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3067-416C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401089 | ||||||
| chr7:74401107
|
G | C | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3067-398G>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401107 | ||||||
| chr7:74401126
|
G | A | 5 | a0001c0001t0004g0058a0002c0003t0002g0177a0002c0006t0002g0023others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-379G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401126 | ||||||
| chr7:74401214
|
A | G | 13 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(10): Show | 13 | HG01081.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3067-291A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401214 | ||||||
| chr7:74401242
|
C | T | 9 | a0001c0001t0001g0047a0001c0001t0007g0146a0001c0001t0007g0147others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3067-263C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401242 | ||||||
| chr7:74401430
|
A | G | 8 | a0001c0001t0002g0133a0001c0001t0002g0182a0001c0001t0002g0272others(5): Show | 8 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.3067-75A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 15/16 | chr7 | 74401430 | ||||||
| chr7:74401593
|
G | T | 2 | a0001c0002t0001g0199a0001c0002t0016g0230 | 2 | HG00408.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3129+26G>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401593 | ||||||
| chr7:74401637
|
C | A | 6 | a0001c0001t0001g0053a0001c0002t0001g0217a0001c0002t0003g0068others(3): Show | 6 | HG01192.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.3129+70C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401637 | ||||||
| chr7:74401637
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3129+70C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401637 | ||||||
| chr7:74401751
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3129+184T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401751 | ||||||
| chr7:74401782
|
T | C | 9 | a0002c0003t0002g0080a0002c0003t0002g0110a0002c0003t0002g0160others(6): Show | 9 | HG00438.hp2 HG01975.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.3129+215T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401782 | ||||||
| chr7:74401820
|
C | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3129+253C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401820 | ||||||
| chr7:74401854
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0014a0001c0001t0006g0016others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3129+287C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401854 | ||||||
| chr7:74401887
|
A | G | 199 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.3129+320A>G | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401887 | ||||||
| chr7:74401895
|
G | A | 12 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0001t0008g0003others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3129+328G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401895 | ||||||
| chr7:74401972
|
T | A | 7 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0007t0007g0013others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3129+405T>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74401972 | ||||||
| chr7:74402098
|
C | T | 8 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0007t0007g0004others(5): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3129+531C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402098 | ||||||
| chr7:74402308
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3129+741C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402308 | ||||||
| chr7:74402329
|
C | CA | 8 | a0001c0001t0001g0144a0001c0001t0006g0014a0001c0001t0008g0003others(5): Show | 8 | HG02071.hp1 HG02683.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.3129+776dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74402329 | |||||
| chr7:74402339
|
A | C | 8 | a0001c0001t0007g0146a0001c0001t0007g0147a0001c0007t0007g0004others(5): Show | 8 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3129+772A>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402339 | ||||||
| chr7:74402344
|
C | A | 1 | a0001c0001t0002g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3129+777C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402344 | ||||||
| chr7:74402345
|
C | CA | 6 | a0001c0001t0001g0087a0001c0001t0001g0154a0001c0002t0001g0097others(3): Show | 6 | HG00673.hp2 HG04184.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.3129+793dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74402345 | |||||
| chr7:74402345
|
CA | C | 20 | a0001c0001t0001g0187a0001c0001t0001g0233a0001c0001t0002g0111others(17): Show | 20 | HG00438.hp1 HG00738.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.3129+793delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74402345 | |||||
| chr7:74402551
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3129+984G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402551 | ||||||
| chr7:74402561
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3129+994G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402561 | ||||||
| chr7:74402743
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3130-1094G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402743 | ||||||
| chr7:74402827
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG02630.hp2 HG02723.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3130-1010G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74402827 | ||||||
| chr7:74403056
|
C | CA | 7 | a0001c0001t0001g0008a0001c0001t0001g0086a0001c0001t0004g0066others(4): Show | 7 | HG01978.hp1 HG01978.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.3130-768dupA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74403056 | |||||
| chr7:74403135
|
CT | C | 182 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.3130-700delT | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74403135 | |||||
| chr7:74403173
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3130-664C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403173 | ||||||
| chr7:74403176
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3130-661G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403176 | ||||||
| chr7:74403214
|
CA | C | 187 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3130-605delA | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 74403214 | |||||
| chr7:74403296
|
C | T | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3130-541C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403296 | ||||||
| chr7:74403414
|
C | A | 1 | a0003c0005t0002g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3130-423C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403414 | ||||||
| chr7:74403421
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3130-416T>C | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403421 | ||||||
| chr7:74403466
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3130-371G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403466 | ||||||
| chr7:74403546
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0007g0146a0001c0001t0007g0147others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3130-291C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403546 | ||||||
| chr7:74403547
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0026a0001c0001t0008g0029others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3130-290G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403547 | ||||||
| chr7:74403615
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3130-222G>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403615 | ||||||
| chr7:74403722
|
C | A | 1 | a0006c0013t0002g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3130-115C>A | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403722 | ||||||
| chr7:74403738
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3130-99C>T | CLIP2 | ENSG00000106665.16 | transcript | ENST00000223398.11 | protein_coding | 16/16 | chr7 | 74403738 |