Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55731 |
|---|---|
| ensemblid | ENSG00000173065.14 |
| hgncid | 25563 |
| symbol | FAM222B |
| name | family with sequence similarity 222 member B |
| refseq_nuc | NM_001077498.3 |
| refseq_prot | NP_001070966.1 |
| ensembl_nuc | ENST00000581407.6 |
| ensembl_prot | ENSP00000462419.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 28755980 |
| end | 28842790 |
| strand | - |
| ver | v1.2 |
| region | chr17:28755980-28842790 |
| region5000 | chr17:28750980-28847790 |
| regionname0 | FAM222B_chr17_28755980_28842790 |
| regionname5000 | FAM222B_chr17_28750980_28847790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 562 | 269 | 72 | 57 | 97 | 6 | 35 | 79 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0002 | 0/0 | 562 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0003 | 0/0 | 562 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0004 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0005 | 0/0 | 562 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0006 | 0/0 | 562 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1689 | 182 | 57 | 40 | 56 | 4 | 24 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0002 | 0/1 | 1689 | 84 | 14 | 15 | 41 | 2 | 11 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0003 | 0/0 | 1689 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0004 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0005 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0006 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0007 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0008 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0009 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| c0010 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2440 | 130 | 33 | 35 | 39 | 4 | 18 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0002 | 0/1 | 2448 | 54 | 13 | 11 | 19 | 1 | 9 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0003 | 0/0 | 2448 | 24 | 0 | 3 | 17 | 1 | 3 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0004 | 0/0 | 2447 | 24 | 13 | 3 | 7 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0005 | 0/0 | 2441 | 12 | 3 | 3 | 6 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0006 | 0/0 | 2449 | 4 | 0 | 0 | 4 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0007 | 0/0 | 2442 | 2 | 1 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0008 | 0/0 | 2441 | 2 | 0 | 1 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0009 | 0/0 | 2440 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0010 | 0/0 | 2440 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0011 | 0/0 | 2440 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0012 | 0/0 | 2447 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0013 | 0/0 | 2447 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0014 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0015 | 0/0 | 2441 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0016 | 0/0 | 2441 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0017 | 0/0 | 2440 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0018 | 0/0 | 2440 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0019 | 0/0 | 2440 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0020 | 0/0 | 2440 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0021 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0022 | 0/0 | 2449 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0023 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0024 | 0/0 | 2448 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0025 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0026 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| t0027 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1689 | 182 | 57 | 40 | 56 | 4 | 24 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002 | 0/1 | 1689 | 84 | 14 | 15 | 41 | 2 | 11 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0006 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0007 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0010 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0002c0003 | 0/0 | 1689 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0003c0004 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0004c0005 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0005c0008 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0006c0009 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4128 | 125 | 30 | 33 | 39 | 4 | 18 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0004 | 0/0 | 4135 | 22 | 12 | 2 | 7 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0005 | 0/0 | 4129 | 11 | 2 | 3 | 6 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0007 | 0/0 | 4130 | 2 | 1 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0008 | 0/0 | 4129 | 2 | 0 | 1 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0009 | 0/0 | 4128 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0010 | 0/0 | 4128 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0011 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0012 | 0/0 | 4135 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0013 | 0/0 | 4135 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0014 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0015 | 0/0 | 4129 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0016 | 0/0 | 4129 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0017 | 0/0 | 4128 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0018 | 0/0 | 4128 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0019 | 0/0 | 4128 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0020 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0021 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0023 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0026 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0001t0027 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0002 | 0/1 | 4136 | 53 | 13 | 10 | 19 | 1 | 9 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0003 | 0/0 | 4136 | 22 | 0 | 3 | 16 | 1 | 2 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0004 | 0/0 | 4135 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0006 | 0/0 | 4137 | 4 | 0 | 0 | 4 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0022 | 0/0 | 4137 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0024 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0002t0025 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0006t0001 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0007t0002 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0001c0010t0001 | 0/0 | 4128 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0002c0003t0001 | 0/0 | 4128 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0003c0004t0001 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0003c0004t0005 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0004c0005t0003 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0005c0008t0003 | 0/0 | 4136 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| a0006c0009t0011 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | copy fasta | chr17 | 28750980 | 28847790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0017g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0018g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0021g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0023g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0026g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0027g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0022g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0024g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0007t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0010t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0002c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0003c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0004c0005t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0005c0008t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0006c0009t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0213 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00738 | hp1 | a0001 | c0010 | t0001 | g0098 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0099 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0165 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01074 | hp1 | a0001 | c0002 | t0025 | g0201 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0197 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0125 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01433 | hp2 | a0001 | c0007 | t0002 | g0208 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0167 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0079 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02055 | hp1 | a0001 | c0001 | t0023 | g0249 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02055 | hp2 | a0003 | c0004 | t0005 | g0027 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | CDX | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0223 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0245 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02683 | hp2 | a0005 | c0008 | t0003 | g0173 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0262 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03041 | hp1 | a0001 | c0001 | t0027 | g0276 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0088 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0205 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03239 | hp1 | a0001 | c0001 | t0017 | g0100 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0067 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0068 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0161 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0261 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03579 | hp1 | a0001 | c0001 | t0021 | g0270 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0236 | SAS | STU | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0214 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03710 | hp1 | a0001 | c0001 | t0016 | g0082 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0219 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | CHB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18947 | hp1 | a0001 | c0002 | t0006 | g0194 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18948 | hp2 | a0001 | c0002 | t0006 | g0206 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18961 | hp2 | a0001 | c0002 | t0022 | g0177 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0117 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18967 | hp1 | a0001 | c0002 | t0006 | g0172 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18974 | hp1 | a0001 | c0002 | t0024 | g0168 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19000 | hp2 | a0004 | c0005 | t0003 | g0192 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19066 | hp1 | a0001 | c0001 | t0019 | g0049 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19066 | hp2 | a0001 | c0001 | t0026 | g0266 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19086 | hp1 | a0001 | c0002 | t0006 | g0200 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0119 | AFR | ASW | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0210 | AFR | ASW | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0231 | EUR | TSI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0271 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG06807 | hp2 | a0006 | c0009 | t0011 | g0004 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0269 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0229 | REF | REF | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0111 | REF | REF | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28758335
|
C | T | 1 | a0003 | 2 | HG02055.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1624G>A | p.Gly542Ser | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1773/4128 | 1624/1689 | 542/562 | chr17 | 28758335 | ||
| chr17:28758379
|
C | T | 1 | a0002 | 2 | HG01243.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1580G>A | p.Arg527Gln | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1729/4128 | 1580/1689 | 527/562 | chr17 | 28758379 | ||
| chr17:28758980
|
T | C | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.979A>G | p.Met327Val | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1128/4128 | 979/1689 | 327/562 | chr17 | 28758980 | ||
| chr17:28759115
|
T | C | 1 | a0006 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.844A>G | p.Ile282Val | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 993/4128 | 844/1689 | 282/562 | chr17 | 28759115 | ||
| chr17:28759600
|
C | T | 1 | a0004 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.359G>A | p.Arg120Gln | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 508/4128 | 359/1689 | 120/562 | chr17 | 28759600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28758546
|
A | G | 4 | a0001c0002a0001c0007a0004c0005others(1): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
synonymous_variant | LOW | c.1413T>C | p.Leu471Leu | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1562/4128 | 1413/1689 | 471/562 | chr17 | 28758546 | ||
| chr17:28758810
|
C | T | 1 | a0001c0006 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1149G>A | p.Thr383Thr | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1298/4128 | 1149/1689 | 383/562 | chr17 | 28758810 | ||
| chr17:28758957
|
G | A | 1 | a0001c0007 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1002C>T | p.Thr334Thr | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1151/4128 | 1002/1689 | 334/562 | chr17 | 28758957 | ||
| chr17:28759182
|
G | A | 1 | a0001c0010 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.777C>T | p.His259His | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 926/4128 | 777/1689 | 259/562 | chr17 | 28759182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28756090
|
T | C | 1 | a0001c0001t0018 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2180A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 2180 | chr17 | 28756090 | |||||
| chr17:28756140
|
G | C | 1 | a0001c0002t0024 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2130C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 2130 | chr17 | 28756140 | |||||
| chr17:28756537
|
G | A | 1 | a0001c0001t0015 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1733 | chr17 | 28756537 | |||||
| chr17:28756570
|
C | T | 2 | a0001c0001t0016a0001c0001t0017 | 2 | HG03239.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1700 | chr17 | 28756570 | |||||
| chr17:28756695
|
T | C | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1575A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1575 | chr17 | 28756695 | |||||
| chr17:28757041
|
T | G | 1 | a0001c0002t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1229 | chr17 | 28757041 | |||||
| chr17:28757207
|
T | G | 1 | a0001c0001t0013 | 2 | HG02965.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1063A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1063 | chr17 | 28757207 | |||||
| chr17:28757270
|
C | A | 1 | a0001c0001t0019 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1000 | chr17 | 28757270 | |||||
| chr17:28757318
|
C | T | 1 | a0001c0001t0026 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 952 | chr17 | 28757318 | |||||
| chr17:28757346
|
T | C | 3 | a0001c0002t0003a0004c0005t0003a0005c0008t0003 | 24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*924A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 924 | chr17 | 28757346 | |||||
| chr17:28757376
|
A | AT | 11 | a0001c0001t0007a0001c0001t0008a0001c0001t0016others(8): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*893dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 893 | chr17 | 28757376 | |||||
| chr17:28757376
|
A | ATT | 2 | a0001c0001t0014a0001c0002t0006 | 5 | HG02615.hp2 NA18947.hp1 NA18948.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*893dupAA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 893 | chr17 | 28757376 | |||||
| chr17:28757391
|
G | A | 1 | a0001c0001t0010 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 879 | chr17 | 28757391 | |||||
| chr17:28757514
|
G | T | 2 | a0001c0001t0012a0001c0001t0021 | 3 | HG02109.hp1 HG03579.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*756C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 756 | chr17 | 28757514 | |||||
| chr17:28757602
|
T | A | 2 | a0001c0001t0011a0006c0009t0011 | 2 | HG03453.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*668A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 668 | chr17 | 28757602 | |||||
| chr17:28757788
|
G | A | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 482 | chr17 | 28757788 | |||||
| chr17:28757854
|
A | AG | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0014others(5): Show | 19 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*415dupC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 415 | chr17 | 28757854 | |||||
| chr17:28842719
|
T | TGCCGCCC | 16 | a0001c0001t0004a0001c0001t0012a0001c0001t0013others(13): Show | 116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-79dupGGGCGGC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/3 | 76053 | chr17 | 28842719 | |||||
| chr17:28842719
|
T | TGCCGCCC others(7): Show |
1 | a0001c0001t0027 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92_-79dupGGGCGGCG others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/3 | 76053 | chr17 | 28842719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28760200
|
A | C | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.83-324T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760200 | ||||||
| chr17:28760247
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.83-371G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760247 | ||||||
| chr17:28760362
|
G | T | 1 | a0001c0001t0020g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-486C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760362 | ||||||
| chr17:28760587
|
G | GA | 89 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0002t0002g0160others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.83-712dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760587 | ||||||
| chr17:28760734
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.83-858C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760734 | ||||||
| chr17:28760911
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.83-1035G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760911 | ||||||
| chr17:28761117
|
G | A | 1 | a0001c0001t0004g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.83-1241C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761117 | ||||||
| chr17:28761298
|
G | A | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83-1422C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761298 | ||||||
| chr17:28761418
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.83-1542G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761418 | ||||||
| chr17:28761488
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-1612G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761488 | ||||||
| chr17:28761583
|
T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.83-1707A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761583 | ||||||
| chr17:28761608
|
C | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.83-1732G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761608 | ||||||
| chr17:28761610
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0083a0001c0001t0007g0072 | 3 | NA18950.hp2 NA18959.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.83-1734G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761610 | ||||||
| chr17:28761805
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0019g0049 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.83-1929T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761805 | ||||||
| chr17:28761891
|
C | T | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.83-2015G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761891 | ||||||
| chr17:28762231
|
G | T | 3 | a0001c0001t0004g0253a0001c0001t0013g0261a0001c0001t0013g0262 | 3 | HG02965.hp1 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.83-2355C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762231 | ||||||
| chr17:28762238
|
C | A | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.83-2362G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762238 | ||||||
| chr17:28762394
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.83-2518C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762394 | ||||||
| chr17:28762403
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.83-2527C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762403 | ||||||
| chr17:28762442
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02602.hp2 HG02698.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2566T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762442 | ||||||
| chr17:28762626
|
CA | C | 204 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.83-2751delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762626 | ||||||
| chr17:28762626
|
CAA | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(12): Show | 15 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-2752_83-2751del others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762626 | ||||||
| chr17:28762839
|
C | G | 6 | a0001c0002t0002g0180a0001c0002t0002g0196a0001c0002t0002g0218others(3): Show | 6 | NA18950.hp1 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2963G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762839 | ||||||
| chr17:28762861
|
C | T | 6 | a0001c0002t0002g0180a0001c0002t0002g0196a0001c0002t0002g0218others(3): Show | 6 | NA18950.hp1 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2985G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762861 | ||||||
| chr17:28762937
|
CA | C | 6 | a0001c0001t0004g0256a0001c0001t0013g0262a0001c0001t0020g0054others(3): Show | 6 | HG01168.hp2 HG02135.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3062delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762937 | ||||||
| chr17:28763212
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.83-3336G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763212 | ||||||
| chr17:28763307
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0093a0001c0001t0001g0101 | 3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+3279A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763307 | ||||||
| chr17:28763406
|
C | T | 1 | a0001c0001t0016g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.82+3180G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763406 | ||||||
| chr17:28763723
|
C | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+2863G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763723 | ||||||
| chr17:28764135
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+2451T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764135 | ||||||
| chr17:28764255
|
G | C | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82+2331C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764255 | ||||||
| chr17:28764271
|
C | CA | 90 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0048others(87): Show | 90 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.82+2314dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | ||||||
| chr17:28764271
|
C | CAA | 12 | a0001c0001t0001g0113a0001c0002t0002g0178a0001c0002t0002g0185others(9): Show | 12 | HG01884.hp1 HG02015.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+2313_82+2314dup others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | ||||||
| chr17:28764271
|
CA | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(19): Show | 22 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.82+2314delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | ||||||
| chr17:28764271
|
CAA | C | 28 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.82+2313_82+2314del others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | ||||||
| chr17:28764294
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.82+2292T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764294 | ||||||
| chr17:28764350
|
G | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82+2236C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764350 | ||||||
| chr17:28764377
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82+2209C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764377 | ||||||
| chr17:28764468
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.82+2118C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764468 | ||||||
| chr17:28764815
|
G | A | 3 | a0001c0002t0002g0207a0001c0002t0002g0237a0001c0002t0002g0245 | 3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+1771C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764815 | ||||||
| chr17:28764933
|
G | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0093others(3): Show | 6 | HG02647.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+1653C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764933 | ||||||
| chr17:28765183
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.82+1403C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765183 | ||||||
| chr17:28765307
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+1279C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765307 | ||||||
| chr17:28765592
|
G | A | 1 | a0001c0001t0007g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82+994C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765592 | ||||||
| chr17:28765685
|
G | C | 2 | a0001c0001t0004g0267a0001c0001t0026g0266 | 2 | NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.82+901C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765685 | ||||||
| chr17:28765776
|
G | C | 30 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(27): Show | 30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.82+810C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765776 | ||||||
| chr17:28765924
|
A | G | 4 | a0001c0002t0002g0180a0001c0002t0002g0196a0001c0002t0006g0200others(1): Show | 4 | NA18961.hp2 NA18966.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+662T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765924 | ||||||
| chr17:28766052
|
G | GAT | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+532_82+533dupAT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766052 | ||||||
| chr17:28766116
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.82+470C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766116 | ||||||
| chr17:28766180
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+406G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766180 | ||||||
| chr17:28766367
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.82+219A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766367 | ||||||
| chr17:28766452
|
C | T | 2 | a0001c0001t0004g0255a0001c0001t0004g0257 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.82+134G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766452 | ||||||
| chr17:28766457
|
T | TA | 8 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0007g0072others(5): Show | 8 | HG01081.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+128dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766457 | ||||||
| chr17:28766457
|
TA | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0005g0057others(4): Show | 7 | HG01070.hp2 HG01099.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+128delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766457 | ||||||
| chr17:28766503
|
C | T | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.82+83G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766503 | ||||||
| chr17:28766524
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(221): Show | 224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.82+62C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766524 | ||||||
| chr17:28766762
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-55C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28766762 | ||||||
| chr17:28766844
|
G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-137C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28766844 | ||||||
| chr17:28767014
|
G | A | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-307C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767014 | ||||||
| chr17:28767062
|
G | GT | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-356dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767062 | ||||||
| chr17:28767349
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009 | 3 | HG01346.hp1 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-40-642C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767349 | ||||||
| chr17:28767401
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-40-694C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767401 | ||||||
| chr17:28767477
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-770G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767477 | ||||||
| chr17:28767778
|
A | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-1071T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767778 | ||||||
| chr17:28767788
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0122 | 2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-1081T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767788 | ||||||
| chr17:28767880
|
A | G | 3 | a0001c0002t0002g0222a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | NA18962.hp1 NA18986.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-40-1173T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767880 | ||||||
| chr17:28768467
|
G | A | 81 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-1760C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768467 | ||||||
| chr17:28768536
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0034 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-40-1829T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768536 | ||||||
| chr17:28768602
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-40-1895G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768602 | ||||||
| chr17:28768615
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0001g0084 | 3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-40-1908A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768615 | ||||||
| chr17:28768810
|
C | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-2103G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768810 | ||||||
| chr17:28768811
|
G | A | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-40-2104C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768811 | ||||||
| chr17:28768836
|
C | CA | 13 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0149others(10): Show | 13 | HG00438.hp1 HG01175.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40-2130dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768836 | ||||||
| chr17:28768836
|
CA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 119 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-40-2130delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768836 | ||||||
| chr17:28768838
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-2131T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768838 | ||||||
| chr17:28769160
|
C | T | 2 | a0001c0002t0002g0220a0001c0002t0004g0205 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-40-2453G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769160 | ||||||
| chr17:28769174
|
C | CT | 137 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-40-2468dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769174 | ||||||
| chr17:28769174
|
C | CTT | 41 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0064others(38): Show | 41 | HG00408.hp2 HG00621.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.-40-2469_-40-2468d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769174 | ||||||
| chr17:28769185
|
T | C | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-2478A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769185 | ||||||
| chr17:28769268
|
T | C | 2 | a0001c0002t0002g0160a0001c0002t0002g0161 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-2561A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769268 | ||||||
| chr17:28769399
|
T | C | 1 | a0001c0002t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-40-2692A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769399 | ||||||
| chr17:28769432
|
C | A | 1 | a0002c0003t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-40-2725G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769432 | ||||||
| chr17:28769433
|
G | A | 1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-40-2726C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769433 | ||||||
| chr17:28769586
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-2879G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769586 | ||||||
| chr17:28769698
|
A | T | 1 | a0001c0001t0026g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-40-2991T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769698 | ||||||
| chr17:28769711
|
G | A | 3 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0026g0266 | 3 | NA18943.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-40-3004C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769711 | ||||||
| chr17:28769772
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0005g0139 | 3 | HG00642.hp1 HG01192.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-40-3065G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769772 | ||||||
| chr17:28770352
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-3645G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770352 | ||||||
| chr17:28770365
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-40-3658A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770365 | ||||||
| chr17:28770446
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-40-3739T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770446 | ||||||
| chr17:28770531
|
C | G | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-3824G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770531 | ||||||
| chr17:28770570
|
TA | T | 85 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-3864delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770570 | ||||||
| chr17:28770571
|
A | AT | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0064others(2): Show | 5 | HG01109.hp2 HG02602.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-3865dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770571 | ||||||
| chr17:28770571
|
A | T | 2 | a0001c0002t0002g0170a0001c0002t0002g0187 | 2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-40-3864T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770571 | ||||||
| chr17:28770593
|
CAG | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-3888_-40-3887d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770593 | ||||||
| chr17:28770640
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-3933C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770640 | ||||||
| chr17:28770663
|
T | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0059others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-3956A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770663 | ||||||
| chr17:28770683
|
G | A | 1 | a0001c0002t0002g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-40-3976C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770683 | ||||||
| chr17:28770871
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0122 | 2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-4164T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770871 | ||||||
| chr17:28770892
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0056 | 2 | HG01109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-40-4185A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770892 | ||||||
| chr17:28770914
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-40-4207A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770914 | ||||||
| chr17:28770940
|
T | TTA | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-4235_-40-4234d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770940 | ||||||
| chr17:28770940
|
TTA | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0141 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-4235_-40-4234d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770940 | ||||||
| chr17:28770952
|
A | G | 2 | a0001c0001t0001g0053a0001c0002t0003g0167 | 2 | HG01496.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-40-4245T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770952 | ||||||
| chr17:28771006
|
A | T | 89 | a0001c0001t0001g0022a0001c0001t0015g0079a0001c0002t0002g0160others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-40-4299T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771006 | ||||||
| chr17:28771013
|
CT | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0043others(19): Show | 22 | HG00738.hp1 HG01123.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-40-4307delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771013 | ||||||
| chr17:28771072
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-4365G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771072 | ||||||
| chr17:28771120
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-40-4413T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771120 | ||||||
| chr17:28771126
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-40-4419T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771126 | ||||||
| chr17:28771637
|
T | C | 1 | a0001c0002t0003g0219 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-40-4930A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771637 | ||||||
| chr17:28771656
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-4949C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771656 | ||||||
| chr17:28771675
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-4968G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771675 | ||||||
| chr17:28772043
|
C | A | 81 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-5336G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772043 | ||||||
| chr17:28772098
|
T | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-5391A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772098 | ||||||
| chr17:28772132
|
C | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0122 | 2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-5425G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772132 | ||||||
| chr17:28772202
|
A | G | 1 | a0001c0002t0002g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-40-5495T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772202 | ||||||
| chr17:28772295
|
C | T | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-5588G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772295 | ||||||
| chr17:28772423
|
C | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-5716G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772423 | ||||||
| chr17:28772495
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-5788G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772495 | ||||||
| chr17:28772560
|
T | TA | 82 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(79): Show | 82 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-40-5854dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772560 | ||||||
| chr17:28772560
|
TA | T | 85 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-5854delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772560 | ||||||
| chr17:28772571
|
T | C | 2 | a0001c0002t0002g0225a0001c0002t0025g0201 | 2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-5864A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772571 | ||||||
| chr17:28772573
|
C | A | 2 | a0001c0002t0002g0225a0001c0002t0025g0201 | 2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-5866G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | ||||||
| chr17:28772573
|
C | CA | 85 | a0001c0001t0001g0075a0001c0001t0001g0136a0001c0002t0002g0160others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-5867dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | ||||||
| chr17:28772573
|
CA | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(53): Show | 56 | HG00408.hp1 HG00544.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-40-5867delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | ||||||
| chr17:28773035
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-40-6328C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773035 | ||||||
| chr17:28773134
|
C | T | 81 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-6427G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773134 | ||||||
| chr17:28773479
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-6772G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | ||||||
| chr17:28773479
|
C | CA | 85 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-40-6773dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | ||||||
| chr17:28773479
|
C | CAA | 12 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0047others(9): Show | 12 | HG00438.hp2 HG01192.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-6774_-40-6773d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | ||||||
| chr17:28773479
|
CA | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0035others(9): Show | 12 | HG01168.hp2 HG02647.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-6773delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | ||||||
| chr17:28773479
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-40-6782_-40-6773d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | ||||||
| chr17:28773534
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-40-6827G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773534 | ||||||
| chr17:28773656
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-40-6949C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773656 | ||||||
| chr17:28773749
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-7042C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773749 | ||||||
| chr17:28773777
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-7070C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773777 | ||||||
| chr17:28773906
|
T | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-7199A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773906 | ||||||
| chr17:28774146
|
C | CT | 96 | a0001c0001t0004g0248a0001c0001t0004g0250a0001c0001t0004g0251others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-40-7440dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774146 | ||||||
| chr17:28774233
|
C | T | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-7526G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774233 | ||||||
| chr17:28774385
|
C | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-7678G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774385 | ||||||
| chr17:28774738
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-40-8031G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774738 | ||||||
| chr17:28774954
|
T | TTAAA | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(5): Show | 8 | HG01346.hp1 HG02258.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-8251_-40-8248d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774954 | ||||||
| chr17:28774957
|
A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-8250T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774957 | ||||||
| chr17:28775003
|
A | AT | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-40-8297dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | ||||||
| chr17:28775003
|
A | ATT | 93 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-40-8298_-40-8297d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | ||||||
| chr17:28775003
|
A | ATTT | 11 | a0001c0002t0002g0179a0001c0002t0002g0198a0001c0002t0002g0202others(8): Show | 11 | HG01346.hp2 HG02132.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40-8299_-40-8297d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | ||||||
| chr17:28775147
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-8440A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775147 | ||||||
| chr17:28775229
|
C | G | 30 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(27): Show | 30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-8522G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775229 | ||||||
| chr17:28775274
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-40-8567G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775274 | ||||||
| chr17:28775275
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-40-8568C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775275 | ||||||
| chr17:28775282
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-40-8575G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775282 | ||||||
| chr17:28775461
|
C | CA | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0135others(4): Show | 7 | HG02055.hp2 HG02602.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-8755dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775461 | ||||||
| chr17:28775461
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-40-8755delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775461 | ||||||
| chr17:28775475
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-8768T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775475 | ||||||
| chr17:28775602
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.-40-8895T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775602 | ||||||
| chr17:28776080
|
A | G | 1 | a0003c0004t0005g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40-9373T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776080 | ||||||
| chr17:28776325
|
G | A | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-40-9618C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776325 | ||||||
| chr17:28776375
|
C | CA | 102 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(99): Show | 102 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-40-9669dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | ||||||
| chr17:28776375
|
C | CAA | 34 | a0001c0001t0001g0060a0001c0001t0004g0259a0001c0001t0004g0274others(31): Show | 34 | HG00544.hp2 HG00642.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-9670_-40-9669d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | ||||||
| chr17:28776375
|
C | CAAA | 7 | a0001c0002t0002g0230a0001c0002t0002g0232a0001c0002t0002g0233others(4): Show | 7 | HG02135.hp1 NA18952.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-9671_-40-9669d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | ||||||
| chr17:28776442
|
C | A | 2 | a0001c0002t0002g0174a0001c0007t0002g0208 | 2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40-9735G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776442 | ||||||
| chr17:28776452
|
C | CT | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40-9746dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | ||||||
| chr17:28776452
|
C | CTT | 5 | a0001c0001t0001g0043a0001c0001t0001g0149a0001c0001t0001g0152others(2): Show | 5 | HG01361.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-9747_-40-9746d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | ||||||
| chr17:28776452
|
CT | C | 89 | a0001c0001t0001g0021a0001c0001t0004g0162a0001c0001t0004g0247others(86): Show | 89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-40-9746delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | ||||||
| chr17:28776629
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-9922T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776629 | ||||||
| chr17:28777225
|
C | T | 1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-40-10518G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777225 | ||||||
| chr17:28777522
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-10815T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777522 | ||||||
| chr17:28777782
|
C | CT | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-11076dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777782 | ||||||
| chr17:28778007
|
C | CT | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(122): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-40-11301dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778007 | ||||||
| chr17:28778007
|
CT | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0075others(4): Show | 7 | HG00099.hp1 HG02015.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-11301delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778007 | ||||||
| chr17:28778028
|
T | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-11321A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778028 | ||||||
| chr17:28778050
|
A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-11343T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778050 | ||||||
| chr17:28778206
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-40-11499A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778206 | ||||||
| chr17:28778343
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-40-11636C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778343 | ||||||
| chr17:28778501
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-11794G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778501 | ||||||
| chr17:28778507
|
C | T | 2 | a0001c0002t0002g0225a0001c0002t0025g0201 | 2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-11800G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778507 | ||||||
| chr17:28778662
|
C | A | 81 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-11955G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778662 | ||||||
| chr17:28778662
|
CCTAG | C | 3 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0221 | 3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-11959_-40-1195 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778662 | ||||||
| chr17:28778670
|
A | AT | 14 | a0001c0002t0002g0164a0001c0002t0002g0169a0001c0002t0002g0170others(11): Show | 14 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40-11964dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778670 | ||||||
| chr17:28778670
|
A | T | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-11963T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778670 | ||||||
| chr17:28778677
|
T | TGTG | 3 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0221 | 3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-11971_-40-1197 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778677 | ||||||
| chr17:28778679
|
T | G | 7 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG03017.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-11972A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778679 | ||||||
| chr17:28778680
|
TG | T | 62 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0002t0002g0166others(59): Show | 62 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-40-11974delC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778680 | ||||||
| chr17:28778680
|
TGTG | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0114 | 3 | NA18951.hp2 NA18952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-40-11976_-40-1197 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778680 | ||||||
| chr17:28778681
|
G | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-40-11974C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778681 | ||||||
| chr17:28778683
|
G | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0144others(8): Show | 11 | HG01168.hp2 HG02135.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40-11976C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778683 | ||||||
| chr17:28778685
|
G | T | 2 | a0001c0001t0001g0144a0001c0002t0002g0224 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-40-11978C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778685 | ||||||
| chr17:28778695
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0004g0248a0001c0001t0013g0261others(1): Show | 4 | HG02258.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-11988C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778695 | ||||||
| chr17:28778695
|
G | GTATATAT others(7): Show |
1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-11989_-40-1198 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778695 | ||||||
| chr17:28778697
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(45): Show | 48 | HG00408.hp1 HG00642.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-40-11990C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778697 | ||||||
| chr17:28778697
|
GTA | G | 34 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-11992_-40-1199 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778697 | ||||||
| chr17:28778699
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0114others(2): Show | 5 | HG01074.hp2 HG03195.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-11992T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778699 | ||||||
| chr17:28778717
|
A | T | 1 | a0001c0002t0002g0228 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-12010T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778717 | ||||||
| chr17:28778718
|
TA | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0133a0001c0001t0001g0134others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-12012delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778718 | ||||||
| chr17:28778719
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0003g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0006g0200 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(31): Show |
1 | a0001c0002t0002g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(42): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(21): Show |
2 | a0001c0002t0002g0171a0001c0002t0003g0240 | 2 | NA19085.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(25): Show |
2 | a0001c0002t0002g0234a0001c0002t0003g0183 | 2 | NA18946.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(27): Show |
2 | a0001c0002t0002g0224a0001c0002t0025g0201 | 2 | HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(19): Show |
2 | a0001c0002t0002g0238a0001c0002t0003g0186 | 2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(20): Show |
1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(21): Show |
5 | a0001c0002t0002g0163a0001c0002t0002g0175a0001c0002t0002g0188others(2): Show | 5 | HG00544.hp2 HG02148.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(22): Show |
1 | a0001c0002t0022g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(25): Show |
2 | a0001c0002t0002g0160a0001c0002t0002g0161 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(26): Show |
4 | a0001c0002t0002g0185a0001c0002t0002g0207a0001c0002t0002g0218others(1): Show | 4 | HG02015.hp1 NA18971.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(37): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0166 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(19): Show |
4 | a0001c0002t0002g0231a0001c0002t0003g0181a0001c0002t0003g0182others(1): Show | 4 | HG02132.hp1 NA18953.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(21): Show |
6 | a0001c0002t0002g0209a0001c0002t0002g0232a0001c0002t0003g0189others(3): Show | 6 | HG00140.hp2 HG00408.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(22): Show |
1 | a0001c0002t0002g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(35): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(19): Show |
5 | a0001c0002t0002g0202a0001c0002t0002g0211a0001c0002t0002g0221others(2): Show | 5 | HG01346.hp2 HG02273.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(20): Show |
4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0002g0230others(1): Show | 4 | NA18943.hp1 NA18947.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(21): Show |
3 | a0001c0002t0002g0217a0001c0002t0002g0225a0004c0005t0003g0192 | 3 | HG04184.hp1 NA19000.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(22): Show |
1 | a0001c0002t0004g0197 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(15): Show |
2 | a0001c0002t0002g0179a0001c0002t0006g0206 | 2 | HG03710.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(17): Show |
3 | a0001c0002t0002g0227a0001c0002t0003g0219a0005c0008t0003g0173 | 3 | HG02683.hp2 HG03831.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(19): Show |
5 | a0001c0002t0002g0222a0001c0002t0002g0226a0001c0002t0002g0233others(2): Show | 5 | NA18952.hp1 NA18978.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(21): Show |
1 | a0001c0007t0002g0208 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(19): Show |
3 | a0001c0002t0002g0187a0001c0002t0002g0220a0001c0002t0002g0246 | 3 | HG01884.hp1 HG03139.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0002g0229 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(9): Show |
2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | ATATATAT others(7): Show |
2 | a0001c0002t0003g0184a0001c0002t0003g0243 | 2 | HG02135.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
A | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(9): Show | 12 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-12012T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
AT | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0039others(15): Show | 18 | HG00438.hp2 HG01168.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40-12013delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
ATT | A | 48 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 48 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778719
|
ATTT | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0005g0073others(3): Show | 6 | HG01496.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-12015_-40-1201 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | ||||||
| chr17:28778720
|
T | TA | 5 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0149others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | ||||||
| chr17:28778720
|
T | TATA | 5 | a0001c0001t0001g0010a0001c0001t0004g0267a0001c0001t0004g0268others(2): Show | 5 | HG02970.hp1 HG06807.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | ||||||
| chr17:28778720
|
T | TATATATA others(16): Show |
1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40-12014_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | ||||||
| chr17:28778721
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0090others(11): Show | 14 | HG00621.hp2 HG01934.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-12014A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778721 | ||||||
| chr17:28778722
|
T | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(13): Show | 16 | HG00438.hp2 HG01168.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40-12015A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778722 | ||||||
| chr17:28778723
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0070others(11): Show | 14 | HG00642.hp1 HG01934.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40-12016A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778723 | ||||||
| chr17:28778724
|
T | A | 3 | a0001c0001t0001g0113a0001c0001t0014g0033a0003c0004t0001g0028 | 3 | HG02615.hp2 HG02970.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-40-12017A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778724 | ||||||
| chr17:28778876
|
C | T | 3 | a0001c0001t0004g0260a0001c0001t0004g0263a0001c0001t0004g0272 | 3 | NA18947.hp2 NA19054.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-40-12169G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778876 | ||||||
| chr17:28778896
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-12189C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778896 | ||||||
| chr17:28778898
|
T | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-12191A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778898 | ||||||
| chr17:28778923
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-12216C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778923 | ||||||
| chr17:28779148
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-40-12441G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779148 | ||||||
| chr17:28779327
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-12620A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779327 | ||||||
| chr17:28779623
|
C | T | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-12916G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779623 | ||||||
| chr17:28779743
|
T | G | 9 | a0001c0001t0004g0260a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG00408.hp1 HG02602.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-13036A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779743 | ||||||
| chr17:28779751
|
A | AAAAT | 87 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0086others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-13048_-40-1304 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779751
|
A | AAAATAAA others(1): Show |
16 | a0001c0001t0001g0140a0001c0001t0004g0267a0001c0001t0004g0268others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.-40-13052_-40-1304 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779751
|
A | AAAATAAA others(5): Show |
2 | a0001c0002t0002g0166a0001c0002t0022g0177 | 2 | HG02293.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-40-13056_-40-1304 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779751
|
A | AATCAATA others(3): Show |
1 | a0001c0002t0003g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-40-13045_-40-1304 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779751
|
AAAATAAA others(5): Show |
A | 5 | a0001c0001t0005g0102a0001c0001t0012g0269a0001c0001t0012g0271others(2): Show | 5 | HG02109.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-13056_-40-1304 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779751
|
AAAATAAA others(9): Show |
A | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-13060_-40-1304 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | ||||||
| chr17:28779795
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-13088C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779795 | ||||||
| chr17:28779800
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-40-13093A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779800 | ||||||
| chr17:28779854
|
C | G | 118 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(115): Show | 118 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-40-13147G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779854 | ||||||
| chr17:28779884
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-13177G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779884 | ||||||
| chr17:28779975
|
CT | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-13269delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779975 | ||||||
| chr17:28780007
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-13300C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780007 | ||||||
| chr17:28780099
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-13392C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780099 | ||||||
| chr17:28780191
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0005g0073 | 2 | NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-40-13484G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780191 | ||||||
| chr17:28780192
|
G | A | 2 | a0003c0004t0001g0028a0003c0004t0005g0027 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40-13485C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780192 | ||||||
| chr17:28780197
|
C | T | 2 | a0001c0001t0011g0003a0006c0009t0011g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-40-13490G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780197 | ||||||
| chr17:28780257
|
G | T | 1 | a0001c0002t0004g0197 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-40-13550C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780257 | ||||||
| chr17:28780338
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-13631G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780338 | ||||||
| chr17:28780362
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-13655A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780362 | ||||||
| chr17:28780427
|
T | A | 2 | a0001c0002t0002g0179a0001c0002t0002g0236 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-40-13720A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780427 | ||||||
| chr17:28780538
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-40-13831C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780538 | ||||||
| chr17:28780832
|
A | C | 1 | a0001c0001t0005g0057 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-40-14125T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780832 | ||||||
| chr17:28780841
|
C | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-14134G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780841 | ||||||
| chr17:28781114
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-14407G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781114 | ||||||
| chr17:28781301
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-40-14594T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781301 | ||||||
| chr17:28781329
|
T | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-14622A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781329 | ||||||
| chr17:28781368
|
A | AAT | 12 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0043others(9): Show | 12 | HG02015.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-14663_-40-1466 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781368 | ||||||
| chr17:28781498
|
A | G | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-14791T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781498 | ||||||
| chr17:28781627
|
C | A | 4 | a0001c0002t0003g0176a0001c0002t0003g0189a0001c0002t0003g0190others(1): Show | 4 | HG00408.hp2 HG02015.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-14920G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781627 | ||||||
| chr17:28781810
|
G | A | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-15103C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781810 | ||||||
| chr17:28782035
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-40-15328T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782035 | ||||||
| chr17:28782512
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-15805T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782512 | ||||||
| chr17:28782861
|
G | C | 1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-40-16154C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782861 | ||||||
| chr17:28782934
|
G | A | 1 | a0001c0002t0002g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-40-16227C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782934 | ||||||
| chr17:28782995
|
G | A | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-40-16288C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782995 | ||||||
| chr17:28783006
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-16299A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783006 | ||||||
| chr17:28783137
|
C | CA | 19 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0077others(16): Show | 19 | HG01106.hp2 HG01361.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-40-16431dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783137 | ||||||
| chr17:28783377
|
G | A | 1 | a0001c0001t0017g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-40-16670C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783377 | ||||||
| chr17:28783499
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0059others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-16792G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783499 | ||||||
| chr17:28783508
|
CATGAG | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-16806_-40-1680 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783508 | ||||||
| chr17:28783533
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40-16826T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783533 | ||||||
| chr17:28783536
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40-16829T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783536 | ||||||
| chr17:28783574
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40-16867T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783574 | ||||||
| chr17:28783576
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40-16869T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783576 | ||||||
| chr17:28783615
|
G | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40-16908C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783615 | ||||||
| chr17:28783924
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-40-17217T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783924 | ||||||
| chr17:28784046
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0020g0054 | 3 | HG02976.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-17339G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784046 | ||||||
| chr17:28784068
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-17361T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784068 | ||||||
| chr17:28784093
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-17386T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784093 | ||||||
| chr17:28784199
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-40-17492G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784199 | ||||||
| chr17:28784242
|
G | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-17535C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784242 | ||||||
| chr17:28784321
|
A | T | 1 | a0001c0001t0013g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-40-17614T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784321 | ||||||
| chr17:28784444
|
T | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-17737A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784444 | ||||||
| chr17:28784491
|
T | TA | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0020others(37): Show | 40 | HG00099.hp2 HG00438.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-40-17785dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAA | 25 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0029others(22): Show | 25 | HG00733.hp2 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-40-17786_-40-1778 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAA | 6 | a0001c0001t0001g0022a0001c0001t0001g0056a0001c0001t0001g0146others(3): Show | 6 | HG00408.hp1 HG01109.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-17787_-40-1778 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA | 8 | a0001c0001t0001g0060a0001c0001t0001g0087a0001c0001t0001g0118others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-17791_-40-1778 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0038a0001c0001t0007g0104 | 2 | HG03486.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-40-17794_-40-1778 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-40-17796_-40-1778 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(7): Show |
1 | a0001c0010t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-40-17798_-40-1778 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-40-17799_-40-1778 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0069 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-40-17802_-40-1778 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0048 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-40-17807_-40-1778 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAA | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(3): Show | 6 | HG01358.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17790_-40-1778 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG00544.hp1 HG00621.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17792_-40-1778 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(3): Show |
T | 5 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0078others(2): Show | 5 | HG02155.hp1 HG02280.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-17794_-40-1778 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-40-17795_-40-1778 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0001g0096a0001c0001t0001g0144 | 2 | HG01123.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-40-17796_-40-1778 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(6): Show |
T | 10 | a0001c0001t0001g0040a0001c0001t0001g0090a0001c0001t0001g0093others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-17797_-40-1778 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(7): Show |
T | 13 | a0001c0001t0001g0031a0001c0001t0001g0089a0001c0001t0001g0105others(10): Show | 13 | HG01243.hp1 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-40-17798_-40-1778 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0135a0001c0001t0001g0154a0001c0001t0013g0261 | 3 | HG01069.hp2 HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-40-17799_-40-1778 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0002t0002g0228 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-17800_-40-1778 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(10): Show |
T | 3 | a0001c0001t0001g0043a0001c0001t0001g0065a0001c0001t0001g0086 | 3 | HG01192.hp1 HG02015.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-40-17801_-40-1778 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(11): Show |
T | 6 | a0001c0001t0001g0005a0001c0002t0002g0202a0001c0002t0002g0211others(3): Show | 6 | HG01346.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17802_-40-1778 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(12): Show |
T | 78 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0005g0024others(75): Show | 78 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-40-17803_-40-1778 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(13): Show |
T | 7 | a0001c0001t0001g0077a0001c0002t0002g0174a0001c0002t0002g0185others(4): Show | 7 | HG01168.hp2 HG01884.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-17804_-40-1778 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784491
|
TAAAAAAA others(17): Show |
T | 2 | a0001c0001t0001g0053a0001c0001t0001g0083 | 2 | NA18950.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-40-17808_-40-1778 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | ||||||
| chr17:28784536
|
A | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-17829T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784536 | ||||||
| chr17:28784614
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40-17907C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784614 | ||||||
| chr17:28784626
|
C | T | 2 | a0001c0002t0002g0178a0001c0002t0002g0185 | 2 | NA18612.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-40-17919G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784626 | ||||||
| chr17:28784916
|
AT | A | 7 | a0001c0001t0001g0144a0001c0001t0004g0259a0001c0002t0002g0193others(4): Show | 7 | HG01081.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-18210delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784916 | ||||||
| chr17:28784982
|
C | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-18275G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784982 | ||||||
| chr17:28785150
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40-18443G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785150 | ||||||
| chr17:28785197
|
C | CT | 81 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-18491dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785197 | ||||||
| chr17:28785198
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-18491A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785198 | ||||||
| chr17:28785522
|
T | G | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-40-18815A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785522 | ||||||
| chr17:28785537
|
GGAT | G | 4 | a0001c0002t0002g0180a0001c0002t0002g0196a0001c0002t0006g0200others(1): Show | 4 | NA18961.hp2 NA18966.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-18833_-40-1883 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785537 | ||||||
| chr17:28785701
|
AT | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0002t0002g0187others(4): Show | 7 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-18995delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785701 | ||||||
| chr17:28785734
|
C | T | 4 | a0001c0002t0003g0181a0001c0002t0003g0182a0001c0002t0003g0183others(1): Show | 4 | HG02132.hp1 HG02135.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-19027G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785734 | ||||||
| chr17:28786018
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-19311C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786018 | ||||||
| chr17:28786200
|
T | A | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-19493A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786200 | ||||||
| chr17:28786489
|
C | T | 1 | a0001c0001t0020g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-40-19782G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786489 | ||||||
| chr17:28786613
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-40-19906G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786613 | ||||||
| chr17:28786708
|
G | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-20001C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786708 | ||||||
| chr17:28786769
|
T | C | 1 | a0001c0001t0005g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-40-20062A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786769 | ||||||
| chr17:28786792
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-40-20085G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786792 | ||||||
| chr17:28786802
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0001g0084 | 3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-40-20095A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786802 | ||||||
| chr17:28786865
|
C | T | 1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-40-20158G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786865 | ||||||
| chr17:28786894
|
AT | A | 45 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(42): Show | 45 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.-40-20188delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | ||||||
| chr17:28786894
|
ATT | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-40-20189_-40-2018 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | ||||||
| chr17:28786894
|
ATTT | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0075others(5): Show | 8 | HG02258.hp2 HG02647.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-20190_-40-2018 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | ||||||
| chr17:28786894
|
ATTTT | A | 78 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(75): Show | 78 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-40-20191_-40-2018 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | ||||||
| chr17:28786894
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0014a0001c0001t0001g0035 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-40-20197_-40-2018 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | ||||||
| chr17:28786943
|
C | T | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-20236G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786943 | ||||||
| chr17:28786953
|
GGAGTGCA others(13): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-40-20266_-40-2024 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786953 | ||||||
| chr17:28787056
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-20349A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787056 | ||||||
| chr17:28787144
|
A | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.-40-20437T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787144 | ||||||
| chr17:28787466
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-20759C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787466 | ||||||
| chr17:28787474
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-20767T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787474 | ||||||
| chr17:28787568
|
G | GC | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-20862dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787568 | ||||||
| chr17:28787582
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-40-20875C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787582 | ||||||
| chr17:28787741
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40-21034G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787741 | ||||||
| chr17:28787826
|
C | CT | 6 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0001g0083others(3): Show | 6 | HG00099.hp2 HG03831.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-21120dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | ||||||
| chr17:28787826
|
C | CTTTTT | 33 | a0001c0001t0004g0162a0001c0001t0004g0250a0001c0001t0004g0252others(30): Show | 33 | HG00408.hp1 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-40-21124_-40-2112 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | ||||||
| chr17:28787826
|
C | CTTTTTT | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-21125_-40-2112 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | ||||||
| chr17:28787826
|
C | CTTTTTTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0011g0003others(4): Show | 7 | HG00544.hp2 HG01109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-21126_-40-2112 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | ||||||
| chr17:28788551
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0065 | 2 | HG02015.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-40-21844A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788551 | ||||||
| chr17:28788828
|
G | A | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-40-22121C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788828 | ||||||
| chr17:28788843
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-40-22136T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788843 | ||||||
| chr17:28788867
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-40-22160C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788867 | ||||||
| chr17:28788871
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-40-22164T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788871 | ||||||
| chr17:28789079
|
C | CA | 31 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(28): Show | 31 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-40-22373dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | ||||||
| chr17:28789079
|
C | CAA | 7 | a0001c0001t0001g0047a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-22374_-40-2237 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | ||||||
| chr17:28789079
|
CA | C | 30 | a0001c0001t0001g0089a0001c0001t0001g0114a0001c0001t0008g0071others(27): Show | 30 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-22373delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | ||||||
| chr17:28789079
|
CAA | C | 53 | a0001c0002t0002g0163a0001c0002t0002g0164a0001c0002t0002g0169others(50): Show | 53 | HG00544.hp2 HG00642.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.-40-22374_-40-2237 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | ||||||
| chr17:28789116
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40-22409G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789116 | ||||||
| chr17:28789198
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-40-22491A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789198 | ||||||
| chr17:28789200
|
C | CT | 8 | a0001c0001t0001g0080a0001c0001t0001g0144a0001c0001t0007g0104others(5): Show | 8 | HG01074.hp1 HG01168.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-22494dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789200 | ||||||
| chr17:28789200
|
CT | C | 15 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0004g0253others(12): Show | 15 | HG00408.hp1 HG02602.hp1 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-40-22494delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789200 | ||||||
| chr17:28789430
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0130 | 2 | HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-40-22723G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789430 | ||||||
| chr17:28789442
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-22735G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789442 | ||||||
| chr17:28789562
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-40-22855G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789562 | ||||||
| chr17:28789721
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-23014G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789721 | ||||||
| chr17:28789954
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-23247G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789954 | ||||||
| chr17:28790175
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-40-23468T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790175 | ||||||
| chr17:28790208
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40-23501A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790208 | ||||||
| chr17:28790288
|
G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(40): Show | 43 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.-40-23581C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790288 | ||||||
| chr17:28790883
|
A | AAATTTTT others(18): Show |
1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-40-24177_-40-2417 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790883 | ||||||
| chr17:28790883
|
A | AAATTTTT others(20): Show |
1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-40-24177_-40-2417 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790883 | ||||||
| chr17:28790884
|
C | CA | 7 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0007g0072others(4): Show | 7 | HG01074.hp1 HG01081.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CAT | 23 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0066others(20): Show | 23 | HG00408.hp2 HG01070.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATT | 29 | a0001c0001t0001g0064a0001c0001t0001g0144a0001c0001t0004g0250others(26): Show | 29 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTT | 8 | a0001c0001t0001g0159a0001c0001t0004g0255a0001c0001t0004g0257others(5): Show | 8 | HG01168.hp2 HG01175.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTT | 7 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0004g0267others(4): Show | 7 | HG01106.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTT | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(29): Show | 32 | HG00544.hp2 HG01109.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT | 25 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(22): Show | 25 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(1): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0096a0001c0001t0001g0127others(9): Show | 12 | HG00733.hp1 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(2): Show |
4 | a0001c0001t0001g0047a0001c0001t0001g0132a0001c0001t0001g0151others(1): Show | 4 | HG00099.hp2 HG01934.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(3): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0150 | 3 | HG01109.hp2 HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(4): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00621.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(5): Show |
4 | a0001c0001t0001g0152a0001c0001t0009g0147a0001c0001t0012g0269others(1): Show | 4 | HG02622.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(6): Show |
3 | a0001c0001t0004g0253a0001c0001t0005g0052a0001c0001t0013g0261 | 3 | HG03130.hp1 HG03540.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(7): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0086a0001c0001t0001g0108 | 3 | HG01192.hp1 HG01361.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(8): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0009g0148 | 3 | HG02895.hp2 NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(9): Show |
2 | a0001c0001t0001g0059a0001c0001t0004g0247 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(10): Show |
1 | a0001c0001t0004g0260 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(11): Show |
4 | a0001c0001t0001g0048a0001c0001t0004g0263a0001c0001t0004g0272others(1): Show | 4 | HG02965.hp1 NA18947.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(12): Show |
1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(13): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0077others(1): Show | 4 | HG01175.hp1 HG02135.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(14): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0085a0001c0001t0001g0094others(2): Show | 5 | HG01358.hp1 HG02630.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(25): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(15): Show |
1 | a0001c0001t0001g0025 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(16): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG00140.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(18): Show |
2 | a0001c0001t0004g0264a0001c0001t0005g0143 | 2 | HG00408.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(19): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0109 | 3 | HG03688.hp1 HG03834.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(20): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0095a0001c0010t0001g0098 | 3 | HG00738.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(21): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0074 | 2 | HG02273.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CATTTTTT others(24): Show |
1 | a0001c0001t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(35): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18955.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-40-24194_-40-2417 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0129 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-40-24205_-40-2417 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0126 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-40-24206_-40-2417 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
C | T | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-40-24177G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
CTT | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0093others(7): Show | 10 | HG01069.hp2 HG01361.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-24179_-40-2417 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
CTTT | C | 11 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0078others(8): Show | 11 | HG01074.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40-24180_-40-2417 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-24188_-40-2417 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
CTTTTTTT others(6): Show |
C | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(9): Show | 12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24190_-40-2417 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790884
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-24191_-40-2417 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | ||||||
| chr17:28790885
|
T | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0140a0001c0001t0004g0274others(1): Show | 4 | HG02602.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24178A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790885 | ||||||
| chr17:28790886
|
T | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0097a0001c0001t0001g0101others(1): Show | 4 | HG00738.hp2 HG01433.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24179A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790886 | ||||||
| chr17:28790887
|
T | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0093others(7): Show | 10 | HG01069.hp2 HG01361.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-24180A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790887 | ||||||
| chr17:28790888
|
T | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0078others(3): Show | 6 | HG01099.hp2 HG01256.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-24181A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790888 | ||||||
| chr17:28790889
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0004g0162 | 2 | NA18522.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-40-24182A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790889 | ||||||
| chr17:28790890
|
T | A | 3 | a0001c0001t0001g0069a0001c0001t0005g0073a0001c0006t0001g0088 | 3 | HG02300.hp2 HG03195.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-40-24183A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790890 | ||||||
| chr17:28790891
|
T | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0055others(1): Show | 4 | HG00438.hp2 NA18973.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24184A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790891 | ||||||
| chr17:28790892
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-24185A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790892 | ||||||
| chr17:28790893
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-40-24186A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790893 | ||||||
| chr17:28790896
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-24189A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790896 | ||||||
| chr17:28790898
|
T | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(9): Show | 12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24191A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790898 | ||||||
| chr17:28790899
|
T | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-24192A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790899 | ||||||
| chr17:28790915
|
T | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(9): Show | 12 | HG00733.hp1 HG01109.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-24208A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790915 | ||||||
| chr17:28791065
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-24358C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791065 | ||||||
| chr17:28791101
|
G | A | 24 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167others(21): Show | 24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-24394C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791101 | ||||||
| chr17:28791161
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40-24454G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791161 | ||||||
| chr17:28791282
|
A | G | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-40-24575T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791282 | ||||||
| chr17:28791554
|
G | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-24847C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791554 | ||||||
| chr17:28791558
|
GCAAAAAA | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-24858_-40-2485 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791558 | ||||||
| chr17:28791675
|
A | AT | 49 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0044others(46): Show | 49 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-40-24969dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | ||||||
| chr17:28791675
|
A | ATT | 39 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0164others(36): Show | 39 | HG00544.hp2 HG01099.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.-40-24970_-40-2496 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | ||||||
| chr17:28791675
|
A | ATTT | 6 | a0001c0002t0002g0163a0001c0002t0002g0169a0001c0002t0002g0170others(3): Show | 6 | HG00642.hp2 HG01106.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-24971_-40-2496 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | ||||||
| chr17:28791675
|
AT | A | 34 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0136others(31): Show | 34 | HG00408.hp1 HG01069.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-24969delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | ||||||
| chr17:28791737
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0060 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-40-25030T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791737 | ||||||
| chr17:28791767
|
G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(241): Show | 244 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.-40-25060C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791767 | ||||||
| chr17:28791861
|
T | C | 1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-40-25154A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791861 | ||||||
| chr17:28792005
|
T | C | 30 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(27): Show | 30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-25298A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792005 | ||||||
| chr17:28792049
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-25342G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792049 | ||||||
| chr17:28792055
|
T | C | 1 | a0001c0002t0003g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-40-25348A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792055 | ||||||
| chr17:28792082
|
C | T | 1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-40-25375G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792082 | ||||||
| chr17:28792099
|
CAGG | C | 20 | a0001c0002t0002g0171a0001c0002t0002g0175a0001c0002t0002g0188others(17): Show | 20 | HG00544.hp2 HG01346.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-40-25395_-40-2539 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792099 | ||||||
| chr17:28792215
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-25508C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792215 | ||||||
| chr17:28792311
|
C | CA | 77 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-40-25605dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792311 | ||||||
| chr17:28792311
|
CA | C | 89 | a0001c0001t0001g0128a0001c0001t0004g0258a0001c0001t0014g0033others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-40-25605delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792311 | ||||||
| chr17:28792506
|
C | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-25799G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792506 | ||||||
| chr17:28792780
|
C | CA | 14 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0149others(11): Show | 14 | HG01069.hp2 HG01175.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40-26074dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | ||||||
| chr17:28792780
|
CA | C | 89 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0105others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-40-26074delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | ||||||
| chr17:28792780
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-26085_-40-2607 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | ||||||
| chr17:28792795
|
A | G | 79 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-40-26088T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792795 | ||||||
| chr17:28792838
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-26131T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792838 | ||||||
| chr17:28792935
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-40-26228A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792935 | ||||||
| chr17:28793612
|
A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-26905T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793612 | ||||||
| chr17:28793742
|
A | AT | 14 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0040others(11): Show | 14 | HG01243.hp2 HG01361.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-27036dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793742 | ||||||
| chr17:28793742
|
AT | A | 12 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0051others(9): Show | 12 | HG01070.hp1 HG02015.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-27036delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793742 | ||||||
| chr17:28793976
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-27269G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793976 | ||||||
| chr17:28793984
|
G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-27277C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793984 | ||||||
| chr17:28794122
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-40-27415T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794122 | ||||||
| chr17:28794222
|
CT | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-27516delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794222 | ||||||
| chr17:28794355
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0001t0001g0137others(2): Show | 5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-27648C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794355 | ||||||
| chr17:28794376
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-27669A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794376 | ||||||
| chr17:28794381
|
G | A | 2 | a0003c0004t0001g0028a0003c0004t0005g0027 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40-27674C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794381 | ||||||
| chr17:28794542
|
T | G | 2 | a0001c0002t0002g0174a0001c0007t0002g0208 | 2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40-27835A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794542 | ||||||
| chr17:28795039
|
G | C | 24 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167others(21): Show | 24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-28332C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795039 | ||||||
| chr17:28795092
|
C | A | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-28385G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795092 | ||||||
| chr17:28795092
|
C | CA | 6 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0062others(3): Show | 6 | HG01361.hp2 HG01891.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-28386dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795092 | ||||||
| chr17:28795135
|
A | G | 80 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(77): Show | 80 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-40-28428T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795135 | ||||||
| chr17:28795137
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-28430C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795137 | ||||||
| chr17:28795226
|
C | A | 1 | a0001c0001t0015g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-40-28519G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795226 | ||||||
| chr17:28795396
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-28689G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795396 | ||||||
| chr17:28795408
|
C | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-28701G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795408 | ||||||
| chr17:28795805
|
A | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-29098T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795805 | ||||||
| chr17:28795812
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-29105G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795812 | ||||||
| chr17:28795942
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-29235T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795942 | ||||||
| chr17:28796516
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-29809A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796516 | ||||||
| chr17:28796518
|
A | C | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-29811T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796518 | ||||||
| chr17:28796577
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0020g0054 | 3 | HG02976.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-29870G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796577 | ||||||
| chr17:28796660
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-40-29953A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796660 | ||||||
| chr17:28796798
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-40-30091G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796798 | ||||||
| chr17:28796843
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-40-30136A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796843 | ||||||
| chr17:28796876
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-30169A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796876 | ||||||
| chr17:28796994
|
C | CT | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(90): Show | 93 | HG00140.hp2 HG00408.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.-40-30288dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | ||||||
| chr17:28796994
|
C | CTT | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0047others(16): Show | 19 | HG00544.hp2 HG00642.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-40-30289_-40-3028 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | ||||||
| chr17:28796994
|
CT | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0058others(3): Show | 6 | HG01168.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-30288delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | ||||||
| chr17:28797037
|
C | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-30330G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797037 | ||||||
| chr17:28797064
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-30357C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797064 | ||||||
| chr17:28797289
|
G | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-30582C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797289 | ||||||
| chr17:28797618
|
G | T | 2 | a0001c0001t0001g0051a0001c0001t0019g0049 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-40-30911C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797618 | ||||||
| chr17:28797739
|
G | T | 1 | a0001c0001t0005g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-40-31032C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797739 | ||||||
| chr17:28797878
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-31171A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797878 | ||||||
| chr17:28797897
|
C | CA | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-31191dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797897 | ||||||
| chr17:28798117
|
G | C | 1 | a0001c0002t0002g0166 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-40-31410C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798117 | ||||||
| chr17:28798296
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-40-31589G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798296 | ||||||
| chr17:28798449
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-31742T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798449 | ||||||
| chr17:28798639
|
C | CT | 86 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-40-31933dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798639 | ||||||
| chr17:28798640
|
T | C | 1 | a0001c0002t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-40-31933A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798640 | ||||||
| chr17:28798658
|
G | A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-31951C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798658 | ||||||
| chr17:28798774
|
T | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-32067A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798774 | ||||||
| chr17:28798774
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-40-32067A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798774 | ||||||
| chr17:28798892
|
C | G | 1 | a0001c0002t0002g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-40-32185G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798892 | ||||||
| chr17:28798909
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-32202T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798909 | ||||||
| chr17:28798972
|
G | GT | 3 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167 | 3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-40-32266dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798972 | ||||||
| chr17:28798972
|
G | GTT | 82 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(79): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-40-32267_-40-3226 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798972 | ||||||
| chr17:28798975
|
G | T | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-32268C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798975 | ||||||
| chr17:28798986
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-40-32279G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798986 | ||||||
| chr17:28799024
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-32317C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799024 | ||||||
| chr17:28799257
|
GC | G | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG01243.hp1 HG01934.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-32551delG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799257 | ||||||
| chr17:28799297
|
C | CT | 9 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0064others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-32591dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799297 | ||||||
| chr17:28799297
|
CT | C | 87 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0056others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-32591delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799297 | ||||||
| chr17:28799392
|
G | GGTTCAAG others(727): Show |
5 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0074others(2): Show | 5 | HG00738.hp1 HG01358.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-33419_-40-3268 others(738): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799392 | ||||||
| chr17:28799471
|
T | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-32764A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799471 | ||||||
| chr17:28799798
|
A | C | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-40-33091T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799798 | ||||||
| chr17:28800034
|
C | CT | 5 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0053others(2): Show | 5 | HG00438.hp2 HG04184.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-33328dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800034 | ||||||
| chr17:28800034
|
CT | C | 87 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0002t0002g0160others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-33328delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800034 | ||||||
| chr17:28800421
|
G | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-33714C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800421 | ||||||
| chr17:28800853
|
G | GA | 101 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-40-34147dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | ||||||
| chr17:28800853
|
G | GAA | 10 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0061others(7): Show | 10 | HG00438.hp2 HG00544.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-34148_-40-3414 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | ||||||
| chr17:28800853
|
GA | G | 15 | a0001c0001t0001g0010a0001c0001t0004g0250a0001c0001t0004g0251others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40-34147delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | ||||||
| chr17:28800926
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40-34219C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800926 | ||||||
| chr17:28800931
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-34224C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800931 | ||||||
| chr17:28801109
|
A | G | 1 | a0001c0002t0003g0243 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-40-34402T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801109 | ||||||
| chr17:28801128
|
G | A | 4 | a0001c0002t0002g0209a0001c0002t0002g0210a0001c0002t0002g0217others(1): Show | 4 | HG02647.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-34421C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801128 | ||||||
| chr17:28801151
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-34444G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801151 | ||||||
| chr17:28801160
|
GA | G | 9 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0252others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-34454delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801160 | ||||||
| chr17:28801191
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-34484G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801191 | ||||||
| chr17:28801235
|
C | T | 5 | a0001c0002t0002g0178a0001c0002t0002g0185a0001c0002t0002g0225others(2): Show | 5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-34528G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801235 | ||||||
| chr17:28801246
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0056a0001c0001t0001g0059others(1): Show | 4 | HG00099.hp2 HG01081.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-34539C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801246 | ||||||
| chr17:28801310
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0001t0001g0137others(2): Show | 5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-34603C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801310 | ||||||
| chr17:28801316
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-34609A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801316 | ||||||
| chr17:28801385
|
C | G | 1 | a0001c0002t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-40-34678G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801385 | ||||||
| chr17:28801433
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-40-34726C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801433 | ||||||
| chr17:28801451
|
C | CA | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0090others(21): Show | 24 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-34745dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | ||||||
| chr17:28801451
|
CA | C | 18 | a0001c0001t0001g0043a0001c0001t0001g0129a0001c0001t0001g0155others(15): Show | 18 | HG00642.hp1 HG01074.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-40-34745delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | ||||||
| chr17:28801451
|
CAA | C | 76 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(73): Show | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-40-34746_-40-3474 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | ||||||
| chr17:28801466
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0035 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-40-34759T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801466 | ||||||
| chr17:28801620
|
A | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-34913T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801620 | ||||||
| chr17:28802007
|
CA | C | 87 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-35301delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802007 | ||||||
| chr17:28802096
|
C | CT | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(125): Show | 128 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-40-35390dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802096 | ||||||
| chr17:28802111
|
AAG | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-35406_-40-3540 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802111 | ||||||
| chr17:28802534
|
A | T | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-35827T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802534 | ||||||
| chr17:28802544
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-35837T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802544 | ||||||
| chr17:28802619
|
A | G | 28 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-35912T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802619 | ||||||
| chr17:28802810
|
G | A | 8 | a0001c0002t0002g0175a0001c0002t0002g0215a0001c0002t0002g0222others(5): Show | 8 | NA18943.hp1 NA18947.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-36103C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802810 | ||||||
| chr17:28802886
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-36179T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802886 | ||||||
| chr17:28803018
|
T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-36311A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803018 | ||||||
| chr17:28803271
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-36564C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803271 | ||||||
| chr17:28803276
|
G | A | 3 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167 | 3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-40-36569C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803276 | ||||||
| chr17:28803287
|
C | A | 1 | a0001c0001t0004g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-40-36580G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803287 | ||||||
| chr17:28803502
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-36795C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803502 | ||||||
| chr17:28803557
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-40-36850T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803557 | ||||||
| chr17:28803695
|
T | C | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40-36988A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803695 | ||||||
| chr17:28803740
|
G | T | 28 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-37033C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803740 | ||||||
| chr17:28803750
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-40-37043G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803750 | ||||||
| chr17:28803946
|
G | A | 28 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-37239C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803946 | ||||||
| chr17:28803973
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-37266G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803973 | ||||||
| chr17:28803973
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-37266G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803973 | ||||||
| chr17:28803980
|
C | CA | 6 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0005g0102others(3): Show | 6 | HG01346.hp1 HG02015.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-37274dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803980 | ||||||
| chr17:28804077
|
T | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-37370A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804077 | ||||||
| chr17:28804116
|
T | C | 3 | a0001c0001t0012g0269a0001c0001t0012g0271a0001c0001t0021g0270 | 3 | HG02109.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-40-37409A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804116 | ||||||
| chr17:28804168
|
G | C | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40-37461C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804168 | ||||||
| chr17:28804339
|
AT | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0141others(2): Show | 5 | HG01192.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-37633delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804339 | ||||||
| chr17:28804375
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-37668C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804375 | ||||||
| chr17:28804482
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-37775C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804482 | ||||||
| chr17:28804586
|
G | A | 5 | a0001c0002t0002g0178a0001c0002t0002g0185a0001c0002t0002g0225others(2): Show | 5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-37879C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804586 | ||||||
| chr17:28804643
|
G | A | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-37936C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804643 | ||||||
| chr17:28804765
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-41+37917C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804765 | ||||||
| chr17:28804870
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-41+37812T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804870 | ||||||
| chr17:28804979
|
G | A | 2 | a0001c0002t0002g0238a0001c0002t0002g0239 | 2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+37703C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804979 | ||||||
| chr17:28805003
|
G | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+37679C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805003 | ||||||
| chr17:28805087
|
G | A | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+37595C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805087 | ||||||
| chr17:28805140
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0122 | 2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-41+37542A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805140 | ||||||
| chr17:28805182
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-41+37500T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805182 | ||||||
| chr17:28805276
|
G | C | 1 | a0001c0002t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+37406C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805276 | ||||||
| chr17:28805489
|
C | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0074others(2): Show | 5 | HG00738.hp1 HG01358.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+37193G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805489 | ||||||
| chr17:28805620
|
G | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+37062C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805620 | ||||||
| chr17:28805724
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+36958C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805724 | ||||||
| chr17:28805875
|
G | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+36807C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805875 | ||||||
| chr17:28806512
|
T | G | 1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+36170A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806512 | ||||||
| chr17:28806557
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-41+36125C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806557 | ||||||
| chr17:28806672
|
T | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156 | 3 | HG01069.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-41+36010A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806672 | ||||||
| chr17:28806826
|
T | C | 1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-41+35856A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806826 | ||||||
| chr17:28806891
|
A | C | 1 | a0001c0002t0002g0221 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-41+35791T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806891 | ||||||
| chr17:28806936
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0060 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-41+35746T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806936 | ||||||
| chr17:28807085
|
G | A | 2 | a0001c0002t0002g0210a0001c0002t0002g0224 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-41+35597C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807085 | ||||||
| chr17:28807251
|
G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+35431C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807251 | ||||||
| chr17:28807360
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+35322C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807360 | ||||||
| chr17:28807467
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-41+35215G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807467 | ||||||
| chr17:28807693
|
T | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0075 | 2 | HG02698.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-41+34989A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807693 | ||||||
| chr17:28807829
|
G | T | 4 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0252others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+34853C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807829 | ||||||
| chr17:28808343
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0093a0001c0001t0001g0101 | 3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-41+34339A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808343 | ||||||
| chr17:28808708
|
T | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+33974A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808708 | ||||||
| chr17:28808813
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-41+33869A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808813 | ||||||
| chr17:28808880
|
CAA | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156 | 3 | HG01069.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-41+33800_-41+3380 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808880 | ||||||
| chr17:28808952
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+33730C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808952 | ||||||
| chr17:28809082
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-41+33600C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809082 | ||||||
| chr17:28809167
|
A | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0141others(2): Show | 5 | HG01192.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+33515T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809167 | ||||||
| chr17:28809211
|
C | T | 1 | a0004c0005t0003g0192 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-41+33471G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809211 | ||||||
| chr17:28809296
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0076 | 2 | HG02132.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-41+33386T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809296 | ||||||
| chr17:28809352
|
C | CA | 13 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0108others(10): Show | 13 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41+33329dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809352 | ||||||
| chr17:28809352
|
CA | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0060others(6): Show | 9 | HG01071.hp1 HG01081.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+33329delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809352 | ||||||
| chr17:28809674
|
A | G | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+33008T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809674 | ||||||
| chr17:28809942
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-41+32740C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809942 | ||||||
| chr17:28809985
|
G | GT | 7 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0058others(4): Show | 7 | HG02148.hp1 HG02615.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+32696dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809985 | ||||||
| chr17:28809985
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-41+32697C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809985 | ||||||
| chr17:28809995
|
G | T | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-41+32687C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809995 | ||||||
| chr17:28810373
|
C | CTGTTTTA others(103): Show |
1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-41+32199_-41+3230 others(114): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810373 | ||||||
| chr17:28810439
|
CTGTTTTA others(15): Show |
C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 242 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-41+32221_-41+3224 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810439 | ||||||
| chr17:28810984
|
A | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+31698T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810984 | ||||||
| chr17:28811059
|
CA | C | 88 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0014g0033others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+31622delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811059 | ||||||
| chr17:28811229
|
A | G | 1 | a0001c0002t0002g0237 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-41+31453T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811229 | ||||||
| chr17:28811465
|
C | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+31217G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811465 | ||||||
| chr17:28811786
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-41+30896G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811786 | ||||||
| chr17:28811799
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+30883A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811799 | ||||||
| chr17:28811949
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+30733T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811949 | ||||||
| chr17:28811950
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+30732C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811950 | ||||||
| chr17:28811952
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+30730C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811952 | ||||||
| chr17:28811982
|
A | G | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-41+30700T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811982 | ||||||
| chr17:28812065
|
G | GGAAAAAA others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-41+30607_-41+3061 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812065 | ||||||
| chr17:28812075
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-41+30607A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812075 | ||||||
| chr17:28812091
|
C | T | 2 | a0001c0002t0002g0238a0001c0002t0002g0239 | 2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+30591G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812091 | ||||||
| chr17:28812314
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-41+30368C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812314 | ||||||
| chr17:28812416
|
A | AC | 5 | a0001c0001t0001g0120a0001c0001t0001g0135a0001c0001t0008g0099others(2): Show | 5 | HG00738.hp2 HG01934.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+30265dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812416 | ||||||
| chr17:28812593
|
A | G | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-41+30089T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812593 | ||||||
| chr17:28812621
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0122 | 2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-41+30061C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812621 | ||||||
| chr17:28812732
|
C | T | 28 | a0001c0001t0001g0062a0001c0001t0004g0247a0001c0001t0004g0248others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-41+29950G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812732 | ||||||
| chr17:28812770
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29912G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812770 | ||||||
| chr17:28812771
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29911T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812771 | ||||||
| chr17:28812772
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29910G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812772 | ||||||
| chr17:28812794
|
A | AC | 21 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0034others(18): Show | 21 | HG01069.hp2 HG01175.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41+29887dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812794 | ||||||
| chr17:28812816
|
C | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+29866G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812816 | ||||||
| chr17:28812869
|
A | G | 2 | a0001c0001t0004g0267a0001c0001t0026g0266 | 2 | NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-41+29813T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812869 | ||||||
| chr17:28813022
|
C | CGG | 20 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0037others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-41+29658_-41+2965 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGG | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.-41+29657_-41+2965 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGGG | 26 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(23): Show | 26 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-41+29656_-41+2965 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGGGG | 19 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0041others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41+29655_-41+2965 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGGGGG | 18 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0042others(15): Show | 18 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41+29654_-41+2965 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGGGGGG others(3): Show |
1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-41+29650_-41+2965 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813022
|
C | CGGGGGGG others(4): Show |
1 | a0001c0001t0005g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-41+29649_-41+2965 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | ||||||
| chr17:28813028
|
GGGGGGGG others(7): Show |
G | 15 | a0001c0002t0002g0178a0001c0002t0002g0180a0001c0002t0002g0202others(12): Show | 15 | HG01346.hp2 HG01952.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813028 | ||||||
| chr17:28813029
|
GGGGGGGG others(6): Show |
G | 36 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(33): Show | 36 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813029 | ||||||
| chr17:28813030
|
GGGGGGGG others(5): Show |
G | 25 | a0001c0002t0002g0164a0001c0002t0002g0166a0001c0002t0002g0175others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813030 | ||||||
| chr17:28813031
|
GGGGGGGG others(4): Show |
G | 7 | a0001c0002t0002g0207a0001c0002t0002g0217a0001c0002t0003g0183others(4): Show | 7 | HG01074.hp1 HG03225.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813031 | ||||||
| chr17:28813032
|
GGGGGGGG others(3): Show |
G | 3 | a0001c0002t0002g0245a0001c0002t0003g0213a0003c0004t0001g0028 | 3 | HG00140.hp2 HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41+29640_-41+2964 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813032 | ||||||
| chr17:28813040
|
G | GGGGGGGG others(4): Show |
1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-41+29641_-41+2964 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813040 | ||||||
| chr17:28813041
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0015g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-41+29640_-41+2964 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813041 | ||||||
| chr17:28813041
|
G | GGGGGGGG others(8): Show |
1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+29640_-41+2964 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813041 | ||||||
| chr17:28813042
|
A | G | 34 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 34 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.-41+29640T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813042 | ||||||
| chr17:28813044
|
G | A | 2 | a0001c0001t0001g0157a0002c0003t0001g0125 | 2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-41+29638C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813044 | ||||||
| chr17:28813044
|
G | T | 1 | a0001c0002t0002g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-41+29638C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813044 | ||||||
| chr17:28813051
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+29631G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813051 | ||||||
| chr17:28813052
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+29630C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813052 | ||||||
| chr17:28813053
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+29629A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813053 | ||||||
| chr17:28813055
|
G | A | 89 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-41+29627C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813055 | ||||||
| chr17:28813068
|
G | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+29614C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813068 | ||||||
| chr17:28813127
|
C | CA | 12 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(9): Show | 12 | HG01123.hp2 HG01192.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+29554dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813127 | ||||||
| chr17:28813127
|
CA | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(34): Show | 37 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.-41+29554delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813127 | ||||||
| chr17:28813129
|
A | C | 86 | a0001c0001t0001g0059a0001c0002t0002g0160a0001c0002t0002g0161others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+29553T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813129 | ||||||
| chr17:28813131
|
A | C | 2 | a0001c0002t0002g0225a0001c0002t0003g0199 | 2 | HG04184.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-41+29551T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813131 | ||||||
| chr17:28813140
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+29542T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813140 | ||||||
| chr17:28813152
|
C | CA | 17 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0080others(14): Show | 17 | HG01069.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-41+29529dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813152 | ||||||
| chr17:28813152
|
CAA | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+29528_-41+2952 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813152 | ||||||
| chr17:28813322
|
T | C | 2 | a0001c0002t0002g0229a0001c0002t0002g0231 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-41+29360A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813322 | ||||||
| chr17:28813524
|
CT | C | 88 | a0001c0001t0004g0267a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+29157delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813524 | ||||||
| chr17:28813535
|
G | GT | 9 | a0001c0001t0001g0023a0001c0001t0001g0046a0001c0001t0001g0064others(6): Show | 9 | HG00140.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+29146dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813535 | ||||||
| chr17:28813535
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-41+29147C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813535 | ||||||
| chr17:28813702
|
A | AT | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 40 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-41+28979dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813702 | ||||||
| chr17:28813702
|
AT | A | 9 | a0001c0001t0001g0118a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG00408.hp1 HG00438.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41+28979delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813702 | ||||||
| chr17:28813736
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+28946G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813736 | ||||||
| chr17:28813793
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+28889C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813793 | ||||||
| chr17:28813836
|
G | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+28846C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813836 | ||||||
| chr17:28814092
|
A | G | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+28590T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814092 | ||||||
| chr17:28814320
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-41+28362G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814320 | ||||||
| chr17:28814321
|
G | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+28361C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814321 | ||||||
| chr17:28814455
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-41+28227A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814455 | ||||||
| chr17:28814487
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+28195G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814487 | ||||||
| chr17:28814532
|
TAATCTTG others(25): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+28118_-41+2814 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814532 | ||||||
| chr17:28814724
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27958G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814724 | ||||||
| chr17:28814731
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27951A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814731 | ||||||
| chr17:28814758
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27924A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814758 | ||||||
| chr17:28814770
|
C | CT | 26 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0034others(23): Show | 26 | HG01099.hp2 HG01168.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.-41+27911dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814770 | ||||||
| chr17:28814770
|
C | CTT | 81 | a0001c0001t0004g0272a0001c0001t0005g0124a0001c0002t0002g0160others(78): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-41+27910_-41+2791 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814770 | ||||||
| chr17:28814813
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-41+27869T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814813 | ||||||
| chr17:28814842
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27840A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814842 | ||||||
| chr17:28814874
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27808T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814874 | ||||||
| chr17:28814880
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27802A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814880 | ||||||
| chr17:28814881
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27801G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814881 | ||||||
| chr17:28814882
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27800A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814882 | ||||||
| chr17:28814898
|
C | T | 8 | a0001c0002t0002g0175a0001c0002t0002g0215a0001c0002t0002g0222others(5): Show | 8 | NA18943.hp1 NA18947.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+27784G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814898 | ||||||
| chr17:28815026
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-41+27656C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815026 | ||||||
| chr17:28815034
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-41+27648T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815034 | ||||||
| chr17:28815214
|
CT | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-41+27467delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815214 | ||||||
| chr17:28815258
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-41+27424C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815258 | ||||||
| chr17:28815275
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27407C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815275 | ||||||
| chr17:28815350
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27332T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815350 | ||||||
| chr17:28815354
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27328G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815354 | ||||||
| chr17:28815447
|
C | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0084 | 2 | NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-41+27235G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815447 | ||||||
| chr17:28815458
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27224G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815458 | ||||||
| chr17:28815487
|
T | A | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+27195A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815487 | ||||||
| chr17:28815488
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27194T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815488 | ||||||
| chr17:28815497
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27185T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815497 | ||||||
| chr17:28815504
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-41+27178C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815504 | ||||||
| chr17:28815510
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-41+27172C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815510 | ||||||
| chr17:28815547
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27135G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815547 | ||||||
| chr17:28815548
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27134G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815548 | ||||||
| chr17:28815549
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27133T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815549 | ||||||
| chr17:28815550
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27132C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815550 | ||||||
| chr17:28815603
|
G | A | 2 | a0001c0002t0002g0174a0001c0007t0002g0208 | 2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-41+27079C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815603 | ||||||
| chr17:28815655
|
T | C | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+27027A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815655 | ||||||
| chr17:28815668
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27014T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815668 | ||||||
| chr17:28815966
|
CA | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0108a0001c0001t0014g0033others(4): Show | 7 | HG01243.hp2 HG01361.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+26715delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815966 | ||||||
| chr17:28815994
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0130a0001c0001t0004g0253others(2): Show | 5 | HG01123.hp2 HG01261.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+26688C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815994 | ||||||
| chr17:28816023
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26659G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816023 | ||||||
| chr17:28816105
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26577T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816105 | ||||||
| chr17:28816196
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26486C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816196 | ||||||
| chr17:28816215
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26467A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816215 | ||||||
| chr17:28816490
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26192A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816490 | ||||||
| chr17:28816559
|
A | T | 2 | a0001c0001t0004g0268a0001c0001t0014g0033 | 2 | HG02615.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-41+26123T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816559 | ||||||
| chr17:28816562
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26120T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816562 | ||||||
| chr17:28816588
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26094T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816588 | ||||||
| chr17:28816590
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26092A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816590 | ||||||
| chr17:28816753
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+25929C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816753 | ||||||
| chr17:28816757
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25925T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816757 | ||||||
| chr17:28816777
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25905A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816777 | ||||||
| chr17:28816792
|
T | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+25890A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816792 | ||||||
| chr17:28816850
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25832A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816850 | ||||||
| chr17:28816874
|
A | G | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0061others(9): Show | 12 | HG00738.hp1 HG01123.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+25808T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816874 | ||||||
| chr17:28816889
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25793A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816889 | ||||||
| chr17:28816943
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25739T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816943 | ||||||
| chr17:28816951
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25731T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816951 | ||||||
| chr17:28816952
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25730A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816952 | ||||||
| chr17:28816953
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25729T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816953 | ||||||
| chr17:28817054
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+25628T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817054 | ||||||
| chr17:28817323
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25359C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817323 | ||||||
| chr17:28817324
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25358T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817324 | ||||||
| chr17:28817366
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25316A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817366 | ||||||
| chr17:28817367
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25315G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817367 | ||||||
| chr17:28817376
|
G | A | 1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-41+25306C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817376 | ||||||
| chr17:28817411
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25271A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817411 | ||||||
| chr17:28817412
|
CA | C | 94 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0095others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-41+25269delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817412 | ||||||
| chr17:28817489
|
C | G | 1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+25193G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817489 | ||||||
| chr17:28817513
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25169C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817513 | ||||||
| chr17:28817514
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25168T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817514 | ||||||
| chr17:28817515
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25167C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817515 | ||||||
| chr17:28817634
|
G | A | 3 | a0001c0001t0004g0253a0001c0001t0013g0261a0001c0001t0013g0262 | 3 | HG02965.hp1 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-41+25048C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817634 | ||||||
| chr17:28818010
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-41+24672T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818010 | ||||||
| chr17:28818057
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+24625G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818057 | ||||||
| chr17:28818106
|
T | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+24576A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818106 | ||||||
| chr17:28818185
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0122others(1): Show | 4 | HG00438.hp2 NA18961.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+24497C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818185 | ||||||
| chr17:28818254
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-41+24428G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818254 | ||||||
| chr17:28818303
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+24379G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818303 | ||||||
| chr17:28818404
|
T | G | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-41+24278A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818404 | ||||||
| chr17:28818511
|
G | C | 1 | a0001c0002t0003g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-41+24171C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818511 | ||||||
| chr17:28818547
|
GAATAAAA others(6): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-41+24122_-41+2413 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818547 | ||||||
| chr17:28818557
|
AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-41+24113_-41+2412 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818557 | ||||||
| chr17:28819337
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-41+23345T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819337 | ||||||
| chr17:28819371
|
G | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+23311C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819371 | ||||||
| chr17:28819388
|
T | C | 1 | a0001c0002t0006g0200 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-41+23294A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819388 | ||||||
| chr17:28819438
|
G | T | 3 | a0001c0002t0003g0186a0001c0002t0003g0191a0001c0002t0003g0240 | 3 | NA18953.hp2 NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-41+23244C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819438 | ||||||
| chr17:28819479
|
G | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+23203C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819479 | ||||||
| chr17:28819670
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0001g0084 | 3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-41+23012T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819670 | ||||||
| chr17:28820073
|
T | G | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+22609A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820073 | ||||||
| chr17:28820122
|
C | T | 1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-41+22560G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820122 | ||||||
| chr17:28820189
|
T | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+22493A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820189 | ||||||
| chr17:28820230
|
T | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+22452A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820230 | ||||||
| chr17:28820438
|
G | A | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-41+22244C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820438 | ||||||
| chr17:28820636
|
C | CT | 18 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0047others(15): Show | 18 | HG00738.hp1 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-41+22045dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820636 | ||||||
| chr17:28820751
|
G | A | 2 | a0001c0002t0002g0229a0001c0002t0002g0231 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-41+21931C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820751 | ||||||
| chr17:28820806
|
T | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(9): Show | 12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41+21876A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820806 | ||||||
| chr17:28820886
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-41+21796G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820886 | ||||||
| chr17:28820950
|
C | CT | 6 | a0001c0002t0002g0218a0001c0002t0002g0224a0001c0002t0002g0226others(3): Show | 6 | HG00140.hp2 HG01433.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+21731dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820950 | ||||||
| chr17:28820955
|
TA | T | 3 | a0001c0002t0002g0203a0001c0002t0002g0238a0001c0002t0003g0243 | 3 | HG02735.hp1 NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-41+21726delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820955 | ||||||
| chr17:28820956
|
A | T | 84 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(81): Show | 84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-41+21726T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820956 | ||||||
| chr17:28820961
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+21721T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820961 | ||||||
| chr17:28820966
|
T | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0140a0001c0001t0001g0144others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+21716A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820966 | ||||||
| chr17:28820967
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-41+21715A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820967 | ||||||
| chr17:28821014
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+21668T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821014 | ||||||
| chr17:28821139
|
A | G | 2 | a0001c0002t0003g0199a0001c0002t0003g0216 | 2 | NA18969.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-41+21543T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821139 | ||||||
| chr17:28821287
|
T | C | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+21395A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821287 | ||||||
| chr17:28821532
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-41+21150G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821532 | ||||||
| chr17:28821827
|
T | C | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-41+20855A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821827 | ||||||
| chr17:28821944
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-41+20738C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821944 | ||||||
| chr17:28822054
|
T | C | 2 | a0001c0002t0002g0163a0001c0002t0002g0164 | 2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-41+20628A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822054 | ||||||
| chr17:28822123
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-41+20559C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822123 | ||||||
| chr17:28822139
|
A | C | 2 | a0001c0001t0010g0067a0001c0001t0010g0068 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-41+20543T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822139 | ||||||
| chr17:28822169
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+20513C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822169 | ||||||
| chr17:28822170
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-41+20512G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822170 | ||||||
| chr17:28822225
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-41+20457G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822225 | ||||||
| chr17:28822485
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41+20197G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822485 | ||||||
| chr17:28822494
|
A | G | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+20188T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822494 | ||||||
| chr17:28822541
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+20141C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822541 | ||||||
| chr17:28822541
|
G | C | 1 | a0001c0001t0005g0052 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+20141C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822541 | ||||||
| chr17:28822657
|
C | T | 5 | a0001c0002t0002g0178a0001c0002t0002g0185a0001c0002t0002g0225others(2): Show | 5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+20025G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822657 | ||||||
| chr17:28822729
|
G | A | 80 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(77): Show | 80 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-41+19953C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822729 | ||||||
| chr17:28822730
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-41+19952C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822730 | ||||||
| chr17:28822737
|
A | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+19945T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822737 | ||||||
| chr17:28822737
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(8): Show | 11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+19945T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822737 | ||||||
| chr17:28822802
|
C | CA | 21 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0030others(18): Show | 21 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41+19879dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
C | CAA | 15 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0040others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41+19878_-41+1987 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CA | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0048others(5): Show | 8 | HG01099.hp2 HG01123.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41+19879delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0002t0002g0164a0001c0002t0002g0169a0001c0002t0002g0174others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+19872_-41+1987 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0002t0002g0233others(3): Show | 6 | HG01069.hp2 HG02683.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41+19871_-41+1987 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CAAAAAAA others(3): Show |
C | 42 | a0001c0001t0001g0144a0001c0002t0002g0160a0001c0002t0002g0161others(39): Show | 42 | HG00408.hp2 HG01070.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-41+19870_-41+1987 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0001g0155a0001c0002t0002g0178a0001c0002t0002g0188others(7): Show | 10 | HG00544.hp2 HG01074.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+19869_-41+1987 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822802
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+19868_-41+1987 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | ||||||
| chr17:28822819
|
AAAAAAAA others(12): Show |
A | 2 | a0001c0002t0002g0209a0001c0002t0002g0224 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-41+19844_-41+1986 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822819 | ||||||
| chr17:28822820
|
A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19862T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822820 | ||||||
| chr17:28822820
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0002t0002g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-41+19842_-41+1986 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822820 | ||||||
| chr17:28822821
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-41+19844_-41+1986 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822821 | ||||||
| chr17:28822821
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0002g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1986 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822821 | ||||||
| chr17:28822822
|
A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19860T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822822 | ||||||
| chr17:28822822
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0009a0001c0001t0011g0003 | 2 | HG01346.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-41+19842_-41+1985 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822822 | ||||||
| chr17:28822823
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-41+19848_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | ||||||
| chr17:28822823
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-41+19844_-41+1985 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | ||||||
| chr17:28822823
|
AAAAAAAA others(10): Show |
A | 5 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+19842_-41+1985 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | ||||||
| chr17:28822824
|
A | T | 2 | a0001c0002t0002g0229a0001c0002t0002g0231 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-41+19858T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | ||||||
| chr17:28822824
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0002t0002g0179a0001c0002t0002g0230a0001c0002t0002g0236 | 3 | HG03688.hp2 HG03710.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-41+19848_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | ||||||
| chr17:28822824
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0002t0002g0241a0001c0002t0006g0194 | 2 | HG02257.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-41+19846_-41+1985 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | ||||||
| chr17:28822825
|
AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0002t0006g0172 | 3 | HG02895.hp1 HG02896.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-41+19846_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822825 | ||||||
| chr17:28822826
|
A | T | 2 | a0001c0002t0002g0229a0001c0002t0002g0231 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-41+19856T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822826 | ||||||
| chr17:28822826
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-41+19846_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822826 | ||||||
| chr17:28822828
|
A | T | 9 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0229others(6): Show | 9 | HG00642.hp2 HG01106.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41+19854T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | ||||||
| chr17:28822828
|
AAAAAATA others(5): Show |
A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1985 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | ||||||
| chr17:28822828
|
AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | ||||||
| chr17:28822829
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822829 | ||||||
| chr17:28822829
|
AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822829 | ||||||
| chr17:28822830
|
A | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0154others(18): Show | 21 | HG00642.hp2 HG01069.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.-41+19852T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | ||||||
| chr17:28822830
|
AAAATATA others(7): Show |
A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+19838_-41+1985 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | ||||||
| chr17:28822830
|
AAAATATA others(11): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | ||||||
| chr17:28822830
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-41+19832_-41+1985 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | ||||||
| chr17:28822831
|
AAATATAT others(32): Show |
A | 3 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0026g0266 | 3 | NA18943.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-41+19812_-41+1985 others(43): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822831 | ||||||
| chr17:28822832
|
A | AAAAATAT others(4): Show |
1 | a0003c0004t0005g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-41+19849_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
A | AAAATATA others(3): Show |
1 | a0003c0004t0001g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-41+19849_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
A | ATAT | 4 | a0001c0001t0001g0140a0001c0001t0013g0262a0001c0001t0016g0082others(1): Show | 4 | HG02965.hp1 HG03239.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+19849_-41+1985 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
A | ATATAT | 3 | a0001c0001t0004g0260a0001c0001t0004g0263a0001c0001t0004g0264 | 3 | HG00408.hp1 NA18947.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-41+19849_-41+1985 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
A | T | 45 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0089others(42): Show | 45 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-41+19850T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
AAT | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0050others(9): Show | 12 | HG01070.hp1 HG01081.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+19848_-41+1984 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822832
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-41+19832_-41+1984 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | ||||||
| chr17:28822833
|
AT | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0016others(22): Show | 25 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41+19848delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822833 | ||||||
| chr17:28822833
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-41+19830_-41+1984 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822833 | ||||||
| chr17:28822834
|
T | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-41+19848A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822834 | ||||||
| chr17:28822836
|
T | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0042others(21): Show | 24 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-41+19846A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822836 | ||||||
| chr17:28822838
|
T | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0059others(6): Show | 9 | HG01081.hp2 HG02015.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+19844A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822838 | ||||||
| chr17:28822842
|
T | TATATATA others(27): Show |
3 | a0001c0001t0004g0255a0001c0001t0012g0271a0001c0001t0021g0270 | 3 | HG02109.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-41+19839_-41+1984 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822842 | ||||||
| chr17:28822842
|
T | TATATATA others(29): Show |
1 | a0001c0001t0012g0269 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-41+19839_-41+1984 others(40): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822842 | ||||||
| chr17:28822855
|
A | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+19827T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822855 | ||||||
| chr17:28822864
|
T | C | 33 | a0001c0001t0001g0076a0001c0001t0001g0086a0001c0001t0004g0258others(30): Show | 33 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-41+19818A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822864 | ||||||
| chr17:28822864
|
TACACAC | T | 4 | a0001c0002t0002g0209a0001c0002t0002g0210a0001c0002t0002g0217others(1): Show | 4 | HG02647.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+19812_-41+1981 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822864 | ||||||
| chr17:28822872
|
T | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+19810A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822872 | ||||||
| chr17:28822882
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+19800A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822882 | ||||||
| chr17:28822905
|
A | G | 19 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0093others(16): Show | 19 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.-41+19777T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822905 | ||||||
| chr17:28822931
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-41+19751C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822931 | ||||||
| chr17:28823010
|
C | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+19672G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823010 | ||||||
| chr17:28823048
|
T | C | 5 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0001t0001g0137others(2): Show | 5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+19634A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823048 | ||||||
| chr17:28823184
|
A | C | 1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-41+19498T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823184 | ||||||
| chr17:28823362
|
A | AT | 11 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0086others(8): Show | 11 | HG01168.hp2 HG01192.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+19319dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | ||||||
| chr17:28823362
|
A | ATT | 82 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(79): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-41+19318_-41+1931 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | ||||||
| chr17:28823362
|
AT | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0090others(4): Show | 7 | HG01099.hp2 HG01256.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+19319delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | ||||||
| chr17:28823372
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+19310A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823372 | ||||||
| chr17:28823685
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0035 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41+18997A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823685 | ||||||
| chr17:28823732
|
T | C | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+18950A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823732 | ||||||
| chr17:28823875
|
A | AT | 96 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0032others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-41+18806dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823875 | ||||||
| chr17:28824114
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-41+18568A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824114 | ||||||
| chr17:28824181
|
AT | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+18500delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824181 | ||||||
| chr17:28824359
|
AT | A | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+18322delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824359 | ||||||
| chr17:28824480
|
C | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+18202G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824480 | ||||||
| chr17:28824541
|
A | G | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-41+18141T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824541 | ||||||
| chr17:28824834
|
G | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+17848C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824834 | ||||||
| chr17:28824873
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+17809G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824873 | ||||||
| chr17:28825007
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41+17675C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825007 | ||||||
| chr17:28825015
|
T | A | 1 | a0001c0002t0002g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-41+17667A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825015 | ||||||
| chr17:28825161
|
A | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0061others(1): Show | 4 | HG02280.hp2 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+17521T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825161 | ||||||
| chr17:28825293
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-41+17389C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825293 | ||||||
| chr17:28825297
|
G | A | 4 | a0001c0002t0003g0176a0001c0002t0003g0189a0001c0002t0003g0190others(1): Show | 4 | HG00408.hp2 HG02015.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+17385C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825297 | ||||||
| chr17:28825375
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-41+17307C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825375 | ||||||
| chr17:28825433
|
C | CA | 31 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0040others(28): Show | 31 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-41+17248dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825433 | ||||||
| chr17:28825451
|
A | C | 30 | a0001c0001t0001g0154a0001c0001t0004g0162a0001c0001t0004g0247others(27): Show | 30 | HG00408.hp1 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-41+17231T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825451 | ||||||
| chr17:28825652
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+17030A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825652 | ||||||
| chr17:28825666
|
T | C | 3 | a0001c0002t0002g0207a0001c0002t0002g0237a0001c0002t0002g0245 | 3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+17016A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825666 | ||||||
| chr17:28825761
|
T | G | 1 | a0001c0002t0002g0235 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-41+16921A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825761 | ||||||
| chr17:28825836
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+16846G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825836 | ||||||
| chr17:28825851
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-41+16831A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825851 | ||||||
| chr17:28826052
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0005g0139 | 2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-41+16630A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826052 | ||||||
| chr17:28826145
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0018g0117 | 2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-41+16537G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826145 | ||||||
| chr17:28826351
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0141others(1): Show | 4 | HG01192.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+16331A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826351 | ||||||
| chr17:28826522
|
C | T | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-41+16160G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826522 | ||||||
| chr17:28826535
|
G | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+16147C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826535 | ||||||
| chr17:28826586
|
C | T | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-41+16096G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826586 | ||||||
| chr17:28826681
|
C | CA | 8 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0064others(5): Show | 8 | HG01175.hp2 HG01192.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+16000dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | ||||||
| chr17:28826681
|
CA | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0035others(30): Show | 33 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-41+16000delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | ||||||
| chr17:28826681
|
CAA | C | 81 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0002t0002g0160others(78): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-41+15999_-41+1600 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | ||||||
| chr17:28826986
|
T | A | 3 | a0001c0001t0005g0107a0001c0002t0002g0174a0001c0006t0001g0088 | 3 | HG00621.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-41+15696A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826986 | ||||||
| chr17:28827204
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+15478T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28827204 | ||||||
| chr17:28827334
|
G | A | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-41+15348C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28827334 | ||||||
| chr17:28828039
|
C | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(8): Show | 11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+14643G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828039 | ||||||
| chr17:28828040
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-41+14642A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828040 | ||||||
| chr17:28828095
|
A | AT | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-41+14586dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
A | ATT | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0084others(7): Show | 10 | HG00408.hp1 HG01192.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+14585_-41+1458 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
AT | A | 29 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0035others(26): Show | 29 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41+14586delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
ATT | A | 14 | a0001c0002t0002g0187a0001c0002t0002g0193a0001c0002t0002g0198others(11): Show | 14 | HG01884.hp1 HG02683.hp2 HG03225.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41+14585_-41+1458 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
ATTT | A | 64 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(61): Show | 64 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-41+14584_-41+1458 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
ATTTT | A | 7 | a0001c0002t0002g0171a0001c0002t0002g0204a0001c0002t0002g0218others(4): Show | 7 | HG01168.hp2 HG03017.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+14583_-41+1458 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828095
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+14575_-41+1458 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | ||||||
| chr17:28828204
|
G | A | 1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-41+14478C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828204 | ||||||
| chr17:28828568
|
G | GA | 88 | a0001c0001t0001g0056a0001c0001t0004g0274a0001c0001t0005g0102others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+14113dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828568 | ||||||
| chr17:28828574
|
A | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009 | 3 | HG01346.hp1 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-41+14108T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828574 | ||||||
| chr17:28828815
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-41+13867A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828815 | ||||||
| chr17:28828846
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0060 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-41+13836T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828846 | ||||||
| chr17:28829218
|
CT | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-41+13463delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829218 | ||||||
| chr17:28829265
|
A | G | 2 | a0001c0002t0002g0207a0001c0002t0002g0245 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+13417T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829265 | ||||||
| chr17:28829307
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+13375G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829307 | ||||||
| chr17:28829357
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-41+13325C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829357 | ||||||
| chr17:28829497
|
G | A | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+13185C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829497 | ||||||
| chr17:28829706
|
T | C | 8 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0252others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+12976A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829706 | ||||||
| chr17:28829848
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+12834T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829848 | ||||||
| chr17:28829875
|
A | T | 2 | a0003c0004t0001g0028a0003c0004t0005g0027 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41+12807T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829875 | ||||||
| chr17:28830161
|
C | CT | 5 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0115others(2): Show | 5 | HG01109.hp2 HG04184.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+12520dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | ||||||
| chr17:28830161
|
CT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.-41+12520delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | ||||||
| chr17:28830161
|
CTT | C | 85 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+12519_-41+1252 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | ||||||
| chr17:28830344
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+12338A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830344 | ||||||
| chr17:28830389
|
C | A | 1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-41+12293G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830389 | ||||||
| chr17:28830568
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+12114A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830568 | ||||||
| chr17:28830680
|
T | C | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-41+12002A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830680 | ||||||
| chr17:28830759
|
G | A | 5 | a0001c0001t0004g0255a0001c0001t0012g0269a0001c0001t0012g0271others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+11923C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830759 | ||||||
| chr17:28830829
|
A | T | 1 | a0001c0001t0023g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-41+11853T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830829 | ||||||
| chr17:28830834
|
T | A | 1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-41+11848A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830834 | ||||||
| chr17:28830845
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+11837T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830845 | ||||||
| chr17:28830980
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41+11702C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830980 | ||||||
| chr17:28830990
|
CT | C | 110 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-41+11691delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830990 | ||||||
| chr17:28830990
|
CTTTTTTT | C | 69 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(66): Show | 69 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.-41+11685_-41+1169 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830990 | ||||||
| chr17:28830998
|
T | G | 7 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167others(4): Show | 7 | HG01070.hp2 HG01496.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+11684A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830998 | ||||||
| chr17:28830999
|
T | G | 80 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(77): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-41+11683A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830999 | ||||||
| chr17:28831004
|
T | G | 3 | a0001c0002t0002g0207a0001c0002t0002g0237a0001c0002t0002g0245 | 3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+11678A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831004 | ||||||
| chr17:28831014
|
G | C | 1 | a0001c0002t0002g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-41+11668C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831014 | ||||||
| chr17:28831169
|
A | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+11513T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831169 | ||||||
| chr17:28831205
|
A | G | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+11477T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831205 | ||||||
| chr17:28831245
|
C | T | 1 | a0001c0002t0003g0242 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-41+11437G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831245 | ||||||
| chr17:28831330
|
C | T | 2 | a0001c0002t0002g0179a0001c0002t0002g0236 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-41+11352G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831330 | ||||||
| chr17:28831342
|
C | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+11340G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831342 | ||||||
| chr17:28831358
|
C | CACTGTCT others(2): Show |
3 | a0001c0002t0002g0207a0001c0002t0002g0237a0001c0002t0002g0245 | 3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+11315_-41+1132 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831358 | ||||||
| chr17:28831504
|
C | CT | 83 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0048others(80): Show | 83 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-41+11177dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | ||||||
| chr17:28831504
|
C | CTT | 11 | a0001c0002t0002g0160a0001c0002t0002g0175a0001c0002t0002g0180others(8): Show | 11 | HG00544.hp2 HG03225.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+11176_-41+1117 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | ||||||
| chr17:28831504
|
CT | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+11177delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | ||||||
| chr17:28832043
|
AG | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0005g0139 | 3 | HG00642.hp1 HG01192.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-41+10638delC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832043 | ||||||
| chr17:28832497
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-41+10185G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832497 | ||||||
| chr17:28832969
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-41+9713C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832969 | ||||||
| chr17:28833009
|
T | TA | 10 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0037others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+9672dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | ||||||
| chr17:28833009
|
TA | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG01070.hp1 HG01261.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41+9672delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | ||||||
| chr17:28833009
|
TAA | T | 79 | a0001c0002t0002g0161a0001c0002t0002g0163a0001c0002t0002g0164others(76): Show | 79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-41+9671_-41+9672d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | ||||||
| chr17:28833009
|
TAAA | T | 8 | a0001c0002t0002g0160a0001c0002t0002g0178a0001c0002t0002g0218others(5): Show | 8 | HG03490.hp2 HG03491.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+9670_-41+9672d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | ||||||
| chr17:28833240
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+9442A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833240 | ||||||
| chr17:28833301
|
T | C | 9 | a0001c0001t0004g0260a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG00408.hp1 HG02602.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+9381A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833301 | ||||||
| chr17:28833508
|
T | C | 2 | a0001c0002t0002g0238a0001c0002t0002g0239 | 2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+9174A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833508 | ||||||
| chr17:28833612
|
C | CA | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41+9069dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | ||||||
| chr17:28833612
|
C | CAA | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(5): Show | 8 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41+9068_-41+9069d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | ||||||
| chr17:28833612
|
CA | C | 12 | a0001c0001t0004g0162a0001c0001t0004g0253a0001c0001t0004g0263others(9): Show | 12 | HG01884.hp1 HG02965.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+9069delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | ||||||
| chr17:28833612
|
CAA | C | 80 | a0001c0001t0001g0043a0001c0002t0002g0160a0001c0002t0002g0161others(77): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-41+9068_-41+9069d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | ||||||
| chr17:28834120
|
A | G | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+8562T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834120 | ||||||
| chr17:28834269
|
T | C | 1 | a0001c0001t0004g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-41+8413A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834269 | ||||||
| chr17:28834383
|
ATC | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+8297_-41+8298d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834383 | ||||||
| chr17:28834478
|
CT | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+8203delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834478 | ||||||
| chr17:28834700
|
T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41+7982A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834700 | ||||||
| chr17:28834798
|
C | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+7884G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834798 | ||||||
| chr17:28834854
|
A | AT | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0086others(4): Show | 7 | HG01175.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+7827dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834854 | ||||||
| chr17:28834854
|
AT | A | 86 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+7827delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834854 | ||||||
| chr17:28834868
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41+7814A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834868 | ||||||
| chr17:28835024
|
T | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+7658A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTG | 28 | a0001c0001t0001g0019a0001c0001t0001g0112a0001c0001t0001g0113others(25): Show | 28 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-41+7656_-41+7657d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTG | 17 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0036others(14): Show | 17 | HG01074.hp2 HG01123.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-41+7654_-41+7657d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTG | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(11): Show | 14 | HG00140.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-41+7652_-41+7657d others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(1): Show |
18 | a0001c0002t0002g0207a0001c0002t0002g0209a0001c0002t0002g0210others(15): Show | 18 | HG00140.hp2 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41+7650_-41+7657d others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(3): Show |
5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0218others(2): Show | 5 | HG03139.hp1 HG03195.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+7648_-41+7657d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(5): Show |
16 | a0001c0002t0002g0163a0001c0002t0002g0221a0001c0002t0002g0222others(13): Show | 16 | HG02148.hp2 HG02293.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.-41+7646_-41+7657d others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(7): Show |
1 | a0001c0002t0002g0233 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-41+7644_-41+7657d others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(9): Show |
7 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0164others(4): Show | 7 | HG01099.hp1 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+7642_-41+7657d others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
T | TTGTGTGT others(11): Show |
1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+7640_-41+7657d others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTG | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(20): Show | 23 | HG00621.hp1 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41+7656_-41+7657d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTG | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0086others(32): Show | 35 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-41+7654_-41+7657d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTG | T | 76 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(73): Show | 76 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-41+7652_-41+7657d others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+7650_-41+7657d others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0037a0001c0002t0022g0177 | 2 | HG02735.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.-41+7648_-41+7657d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+7646_-41+7657d others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+7644_-41+7657d others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835024
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+7638_-41+7657d others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | ||||||
| chr17:28835085
|
G | A | 1 | a0001c0001t0004g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-41+7597C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835085 | ||||||
| chr17:28835139
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-41+7543C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835139 | ||||||
| chr17:28835162
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-41+7520T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835162 | ||||||
| chr17:28835277
|
C | T | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-41+7405G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835277 | ||||||
| chr17:28835436
|
A | G | 30 | a0001c0001t0004g0162a0001c0001t0004g0247a0001c0001t0004g0248others(27): Show | 30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-41+7246T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835436 | ||||||
| chr17:28835517
|
T | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-41+7165A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835517 | ||||||
| chr17:28835832
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-41+6850G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835832 | ||||||
| chr17:28835838
|
A | AT | 10 | a0001c0001t0001g0036a0001c0001t0004g0250a0001c0001t0004g0251others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+6843dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835838 | ||||||
| chr17:28835856
|
G | C | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+6826C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835856 | ||||||
| chr17:28835993
|
A | AT | 88 | a0001c0001t0014g0033a0001c0002t0002g0160a0001c0002t0002g0161others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+6688dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835993 | ||||||
| chr17:28836240
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-41+6442C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836240 | ||||||
| chr17:28836277
|
C | A | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+6405G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836277 | ||||||
| chr17:28836279
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0035 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41+6403G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836279 | ||||||
| chr17:28836329
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+6353C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836329 | ||||||
| chr17:28836415
|
G | A | 1 | a0001c0002t0002g0237 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-41+6267C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836415 | ||||||
| chr17:28836615
|
G | C | 2 | a0001c0002t0002g0238a0001c0002t0002g0239 | 2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+6067C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836615 | ||||||
| chr17:28836621
|
C | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0141 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-41+6061G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836621 | ||||||
| chr17:28836857
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+5825A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836857 | ||||||
| chr17:28836896
|
T | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+5786A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836896 | ||||||
| chr17:28836996
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-41+5686A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836996 | ||||||
| chr17:28837141
|
A | G | 2 | a0001c0001t0011g0003a0006c0009t0011g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-41+5541T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837141 | ||||||
| chr17:28837199
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-41+5483C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837199 | ||||||
| chr17:28837221
|
G | C | 1 | a0001c0001t0005g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-41+5461C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837221 | ||||||
| chr17:28837413
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+5269C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837413 | ||||||
| chr17:28837436
|
A | T | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+5246T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837436 | ||||||
| chr17:28837440
|
A | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(105): Show | 108 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-41+5242T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837440 | ||||||
| chr17:28837444
|
T | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0005g0024others(1): Show | 4 | HG01099.hp2 HG01123.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+5238A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837444 | ||||||
| chr17:28837549
|
G | A | 1 | a0001c0002t0003g0240 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-41+5133C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837549 | ||||||
| chr17:28837564
|
A | G | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-41+5118T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837564 | ||||||
| chr17:28837646
|
G | GT | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0002g0174others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+5035dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837646 | ||||||
| chr17:28837665
|
T | C | 87 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+5017A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837665 | ||||||
| chr17:28837715
|
T | C | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-41+4967A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837715 | ||||||
| chr17:28837748
|
A | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+4934T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837748 | ||||||
| chr17:28838164
|
CTGAAGCA others(11): Show |
C | 6 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+4500_-41+4517d others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838164 | ||||||
| chr17:28838371
|
G | A | 3 | a0001c0002t0003g0242a0001c0002t0003g0243a0001c0002t0003g0244 | 3 | NA18959.hp1 NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-41+4311C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838371 | ||||||
| chr17:28838574
|
T | A | 1 | a0001c0002t0002g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-41+4108A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838574 | ||||||
| chr17:28838648
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-41+4034A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838648 | ||||||
| chr17:28839122
|
G | A | 1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41+3560C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839122 | ||||||
| chr17:28839123
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-41+3559G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839123 | ||||||
| chr17:28839156
|
G | A | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-41+3526C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839156 | ||||||
| chr17:28839282
|
A | G | 1 | a0001c0002t0002g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-41+3400T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839282 | ||||||
| chr17:28839360
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG00544.hp1 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+3322G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839360 | ||||||
| chr17:28839485
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+3197G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839485 | ||||||
| chr17:28839688
|
A | T | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-41+2994T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839688 | ||||||
| chr17:28840042
|
G | A | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-41+2640C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840042 | ||||||
| chr17:28840048
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(8): Show | 11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+2634C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840048 | ||||||
| chr17:28840149
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-41+2533C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840149 | ||||||
| chr17:28840158
|
C | G | 1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-41+2524G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840158 | ||||||
| chr17:28840318
|
A | C | 1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-41+2364T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840318 | ||||||
| chr17:28840513
|
G | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+2169C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840513 | ||||||
| chr17:28840736
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+1946G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840736 | ||||||
| chr17:28840748
|
G | A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+1934C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840748 | ||||||
| chr17:28840792
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-41+1890A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840792 | ||||||
| chr17:28840831
|
C | T | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+1851G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840831 | ||||||
| chr17:28840910
|
A | C | 89 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0002g0160others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-41+1772T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840910 | ||||||
| chr17:28840955
|
C | G | 89 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0002g0160others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-41+1727G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840955 | ||||||
| chr17:28840960
|
C | G | 3 | a0001c0002t0002g0166a0001c0002t0003g0165a0001c0002t0003g0167 | 3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-41+1722G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840960 | ||||||
| chr17:28841288
|
C | G | 2 | a0001c0002t0002g0163a0001c0002t0002g0164 | 2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-41+1394G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841288 | ||||||
| chr17:28841309
|
T | C | 89 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0002g0160others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-41+1373A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841309 | ||||||
| chr17:28841417
|
C | G | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-41+1265G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841417 | ||||||
| chr17:28841468
|
G | A | 117 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0004g0162others(114): Show | 117 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-41+1214C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841468 | ||||||
| chr17:28841942
|
G | C | 29 | a0001c0001t0004g0247a0001c0001t0004g0248a0001c0001t0004g0250others(26): Show | 29 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41+740C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841942 | ||||||
| chr17:28841994
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-41+688T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841994 | ||||||
| chr17:28842106
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-41+576C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842106 | ||||||
| chr17:28842508
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+174C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842508 | ||||||
| chr17:28842550
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(7): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+132T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842550 | ||||||
| chr17:28842629
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-41+53C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842629 | ||||||
| chr17:28842650
|
G | A | 1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-41+32C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842650 |