Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 151195 |
| ensemblid | ENSG00000163249.13 |
| hgncid | 26868 |
| symbol | CCNYL1 |
| name | cyclin Y like 1 |
| refseq_nuc | NM_001330218.2 |
| refseq_prot | NP_001317147.1 |
| ensembl_nuc | ENST00000295414.8 |
| ensembl_prot | ENSP00000295414.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 207711640 |
| end | 207756174 |
| strand | + |
| ver | v1.2 |
| region | chr2:207711640-207756174 |
| region5000 | chr2:207706640-207761174 |
| regionname0 | CCNYL1_chr2_207711640_207756174 |
| regionname5000 | CCNYL1_chr2_207706640_207761174 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 352 | 88 | 64 | 146 | 14 | 38 | 105 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | MGNTL others(354): Show |
chr2 | 207706640 | 207761174 |
| a0002 | 0/0 | 359 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | MGNTL others(354): Show |
chr2 | 207706640 | 207761174 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 345 | 85 | 63 | 146 | 14 | 35 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | ATGGG others(1072): Show |
chr2 | 207706640 | 207761174 | ||
| a0001c0002 | 0/0 | 1077 | 4 | 0 | 1 | 0 | 0 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | ATGGG others(1072): Show |
chr2 | 207706640 | 207761174 | ||
| a0001c0004 | 0/0 | 1077 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | ATGGG others(1072): Show |
chr2 | 207706640 | 207761174 | ||
| a0001c0005 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | ATGGG others(1072): Show |
chr2 | 207706640 | 207761174 | ||
| a0002c0003 | 0/0 | 1077 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | ATGGG others(1072): Show |
chr2 | 207706640 | 207761174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3814 | 200 | 42 | 32 | 99 | 7 | 19 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0002 | 1/0 | 3813 | 107 | 15 | 26 | 45 | 6 | 14 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0003 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0004 | 0/0 | 3814 | 5 | 0 | 3 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0005 | 0/0 | 3813 | 4 | 4 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0006 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0007 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0008 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0009 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0010 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0011 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0012 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0013 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0014 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0015 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0016 | 0/0 | 3813 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0017 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0018 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0019 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0020 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0021 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0001t0022 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0002t0001 | 0/0 | 3814 | 4 | 0 | 1 | 0 | 0 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0001c0004t0002 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3808): Show |
chr2 | 207706640 | 207761174 |
| a0001c0005t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| a0002c0003t0001 | 0/0 | 3814 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | GCAGA others(3809): Show |
chr2 | 207706640 | 207761174 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0001 | 0/0 | 13 | 0 | 1 | 8 | 1 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0020g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0021g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0001t0022g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0004t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0001c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0124 | EUR | FIN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00408 | hp2 | a0001 | c0001 | t0012 | g0172 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0152 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01884 | hp2 | a0001 | c0001 | t0020 | g0171 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CDX | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02273 | hp1 | a0001 | c0001 | t0010 | g0216 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0029 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0199 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0299 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0300 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02896 | hp1 | a0001 | c0001 | t0019 | g0277 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0298 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0006 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0140 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0207 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0293 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0074 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0131 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0295 | SAS | GIH | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0141 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0248 | REF | REF | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0233 | REF | REF | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207711991 | T | G | 1 | a0002 | 2 | HG02074.hp1 NA18984.hp1 |
missense_variant | MODERATE | c.95T>G | p.Ile32Ser | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/10 | 352/3813 | 95/1080 | 32/359 | chr2 | 207711991 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207712007 | C | T | 1 | a0001c0002 | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.111C>T | p.Ser37Ser | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/10 | 368/3813 | 111/1080 | 37/359 | chr2 | 207712007 | |||
| chr2:207742285 | T | C | 1 | a0001c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.582T>C | p.Phe194Phe | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/10 | 839/3813 | 582/1080 | 194/359 | chr2 | 207742285 | |||
| chr2:207747073 | T | C | 1 | a0001c0004 | 2 | HG02630.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.666T>C | p.Tyr222Tyr | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/10 | 923/3813 | 666/1080 | 222/359 | chr2 | 207747073 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207753755 | A | C | 1 | a0001c0001t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 57 | chr2 | 207753755 | ||||||
| chr2:207753878 | A | G | 1 | a0001c0001t0021 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 180 | chr2 | 207753878 | ||||||
| chr2:207753941 | G | A | 1 | a0001c0001t0008 | 2 | HG02818.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*243G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 243 | chr2 | 207753941 | ||||||
| chr2:207754054 | A | G | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 356 | chr2 | 207754054 | ||||||
| chr2:207754112 | C | G | 2 | a0001c0001t0007 a0001c0001t0019 |
4 | HG02055.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 414 | chr2 | 207754112 | ||||||
| chr2:207754221 | T | TA | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(11): Show |
226 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*524dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 525 | INFO_REALIGN_3_PRIME | chr2 | 207754221 | |||||
| chr2:207754443 | G | C | 1 | a0001c0001t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 745 | chr2 | 207754443 | ||||||
| chr2:207754514 | G | A | 1 | a0001c0001t0010 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 816 | chr2 | 207754514 | ||||||
| chr2:207754672 | A | C | 1 | a0001c0001t0005 | 4 | HG02145.hp2 HG02280.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*974A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 974 | chr2 | 207754672 | ||||||
| chr2:207754916 | G | A | 1 | a0001c0001t0004 | 5 | HG00738.hp1 HG01361.hp2 HG01981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1218G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1218 | chr2 | 207754916 | ||||||
| chr2:207754988 | G | A | 1 | a0001c0001t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1290 | chr2 | 207754988 | ||||||
| chr2:207755056 | C | G | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1358 | chr2 | 207755056 | ||||||
| chr2:207755350 | A | G | 1 | a0001c0001t0018 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1652A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1652 | chr2 | 207755350 | ||||||
| chr2:207755358 | C | T | 1 | a0001c0001t0006 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1660C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1660 | chr2 | 207755358 | ||||||
| chr2:207755854 | C | G | 1 | a0001c0001t0012 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2156C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2156 | chr2 | 207755854 | ||||||
| chr2:207755892 | A | C | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2194 | chr2 | 207755892 | ||||||
| chr2:207755923 | A | G | 1 | a0001c0001t0011 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2225 | chr2 | 207755923 | ||||||
| chr2:207755932 | A | G | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0019 |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2234 | chr2 | 207755932 | ||||||
| chr2:207756013 | T | A | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2315T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2315 | chr2 | 207756013 | ||||||
| chr2:207756099 | A | G | 1 | a0001c0001t0016 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2401A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2401 | chr2 | 207756099 | ||||||
| chr2:207756102 | G | T | 1 | a0001c0001t0009 | 2 | HG02486.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2404G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2404 | chr2 | 207756102 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207712294 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.220+178A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712294 | |||||||
| chr2:207712407 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+291A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712407 | |||||||
| chr2:207712440 | G | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+324G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712440 | |||||||
| chr2:207712670 | A | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0300 a0001c0005t0001g0298 |
3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+554A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712670 | |||||||
| chr2:207712834 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.220+718C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712834 | |||||||
| chr2:207712859 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.220+743A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712859 | |||||||
| chr2:207712889 | C | T | 2 | a0001c0001t0008g0299 a0001c0001t0008g0300 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.220+773C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712889 | |||||||
| chr2:207712932 | C | T | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+816C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712932 | |||||||
| chr2:207713114 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+998G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713114 | |||||||
| chr2:207713172 | G | A | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+1056G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713172 | |||||||
| chr2:207713306 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+1190G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713306 | |||||||
| chr2:207713310 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220+1194T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713310 | |||||||
| chr2:207713687 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.220+1571A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713687 | |||||||
| chr2:207713745 | C | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+1629C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713745 | |||||||
| chr2:207713765 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+1649T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713765 | |||||||
| chr2:207713787 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.220+1671A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713787 | |||||||
| chr2:207713803 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.220+1687T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713803 | |||||||
| chr2:207713811 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.220+1695T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713811 | |||||||
| chr2:207713996 | A | G | 1 | a0001c0001t0002g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.220+1880A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713996 | |||||||
| chr2:207713996 | ATACTTTC others(3): Show |
A | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+1884_220+1893d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207713996 | ||||||
| chr2:207714058 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+1942G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714058 | |||||||
| chr2:207714312 | C | CT | 13 | a0001c0001t0001g0120 a0001c0001t0001g0280 a0001c0001t0001g0281 others(10): Show |
15 | HG00438.hp2 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.220+2222dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714312 | CT | C | 50 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0035 others(47): Show |
54 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.220+2222delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714312 | CTT | C | 16 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(13): Show |
16 | HG00323.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+2221_220+2222d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714312 | CTTT | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
84 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.220+2220_220+2222d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714312 | CTTTT | C | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
18 | HG01069.hp1 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.220+2219_220+2222d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714312 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.220+2212_220+2222d others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | ||||||
| chr2:207714442 | G | A | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220+2326G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714442 | |||||||
| chr2:207714632 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+2516A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714632 | |||||||
| chr2:207714667 | G | GATGATGA others(3): Show |
1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+2553_220+2562d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714667 | ||||||
| chr2:207714836 | G | A | 1 | a0001c0001t0012g0172 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.220+2720G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714836 | |||||||
| chr2:207715028 | G | T | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+2912G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715028 | |||||||
| chr2:207715045 | G | A | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+2929G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715045 | |||||||
| chr2:207715096 | C | T | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+2980C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715096 | |||||||
| chr2:207715097 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA19064.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.220+2981G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715097 | |||||||
| chr2:207715268 | AAAAC | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
201 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.220+3168_220+3171d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715268 | ||||||
| chr2:207715339 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+3223C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715339 | |||||||
| chr2:207715379 | C | CT | 101 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(98): Show |
112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.220+3285dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | ||||||
| chr2:207715379 | C | CTT | 86 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0039 others(83): Show |
110 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.220+3284_220+3285d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | ||||||
| chr2:207715379 | C | CTTT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
98 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.220+3283_220+3285d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | ||||||
| chr2:207715379 | C | CTTTT | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00597.hp2 HG02027.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+3282_220+3285d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | ||||||
| chr2:207715379 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.220+3274_220+3285d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | ||||||
| chr2:207715436 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+3320A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715436 | |||||||
| chr2:207715473 | G | A | 3 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 |
3 | NA18944.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.220+3357G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715473 | |||||||
| chr2:207715511 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+3395T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715511 | |||||||
| chr2:207715624 | G | T | 6 | a0001c0001t0002g0166 a0001c0001t0002g0265 a0001c0001t0002g0266 others(3): Show |
6 | HG02015.hp1 HG03831.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+3508G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715624 | |||||||
| chr2:207715676 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+3560G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715676 | |||||||
| chr2:207715679 | C | CT | 10 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(7): Show |
11 | HG01192.hp2 HG01261.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+3577dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715679 | ||||||
| chr2:207715679 | CT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+3577delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715679 | ||||||
| chr2:207715696 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG00544.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.220+3580G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715696 | |||||||
| chr2:207715745 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(89): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.220+3629C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715745 | |||||||
| chr2:207715843 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0104 others(1): Show |
4 | HG02735.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+3727A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715843 | |||||||
| chr2:207716106 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.220+3990A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716106 | |||||||
| chr2:207716312 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.220+4196C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716312 | |||||||
| chr2:207716339 | C | CT | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0099 others(6): Show |
9 | HG00438.hp1 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+4239dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207716339 | ||||||
| chr2:207716339 | CT | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(94): Show |
106 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.220+4239delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207716339 | ||||||
| chr2:207716459 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.220+4343A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716459 | |||||||
| chr2:207716574 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.220+4458C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716574 | |||||||
| chr2:207716584 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.220+4468G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716584 | |||||||
| chr2:207716656 | T | C | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.220+4540T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716656 | |||||||
| chr2:207716662 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.220+4546A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716662 | |||||||
| chr2:207716715 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): Show |
102 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.220+4599C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716715 | |||||||
| chr2:207716739 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220+4623G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716739 | |||||||
| chr2:207716848 | G | A | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+4732G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716848 | |||||||
| chr2:207716881 | G | C | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+4765G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716881 | |||||||
| chr2:207716912 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0122 a0001c0001t0002g0142 others(2): Show |
6 | HG01243.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+4796A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716912 | |||||||
| chr2:207716926 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.220+4810G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716926 | |||||||
| chr2:207717108 | C | CA | 32 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(29): Show |
33 | HG00438.hp1 HG00597.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.220+5011dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207717108 | ||||||
| chr2:207717254 | T | C | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+5138T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717254 | |||||||
| chr2:207717428 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+5312G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717428 | |||||||
| chr2:207717435 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+5319G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717435 | |||||||
| chr2:207717492 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+5376G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717492 | |||||||
| chr2:207717625 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.220+5509G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717625 | |||||||
| chr2:207717773 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.220+5657G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717773 | |||||||
| chr2:207717799 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.220+5683A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717799 | |||||||
| chr2:207717906 | C | CT | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.220+5805dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207717906 | ||||||
| chr2:207717943 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0225 |
4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+5827C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717943 | |||||||
| chr2:207717946 | C | T | 1 | a0001c0001t0002g0026 | 2 | NA18957.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.220+5830C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717946 | |||||||
| chr2:207718007 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220+5891C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718007 | |||||||
| chr2:207718008 | G | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+5892G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718008 | |||||||
| chr2:207718017 | G | A | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+5901G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718017 | |||||||
| chr2:207718088 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+5972T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718088 | |||||||
| chr2:207718127 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0045 others(4): Show |
10 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+6011A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718127 | |||||||
| chr2:207718161 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+6045C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718161 | |||||||
| chr2:207718200 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.220+6084G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718200 | |||||||
| chr2:207718251 | A | G | 2 | a0001c0001t0002g0122 a0001c0001t0002g0301 |
2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.220+6135A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718251 | |||||||
| chr2:207718323 | A | G | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+6207A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718323 | |||||||
| chr2:207718349 | A | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.220+6233A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718349 | |||||||
| chr2:207718356 | A | G | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+6240A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718356 | |||||||
| chr2:207718429 | G | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+6313G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718429 | |||||||
| chr2:207718468 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0264 |
2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.221-6332A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718468 | |||||||
| chr2:207718503 | C | CA | 6 | a0001c0001t0001g0120 a0001c0001t0001g0235 a0001c0001t0002g0263 others(3): Show |
6 | HG01981.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-6284dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718503 | ||||||
| chr2:207718704 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.221-6096G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718704 | |||||||
| chr2:207718805 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.221-5995A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718805 | |||||||
| chr2:207718831 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221-5969A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718831 | |||||||
| chr2:207718906 | A | G | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.221-5894A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718906 | |||||||
| chr2:207718975 | T | TA | 8 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(5): Show |
9 | HG00733.hp2 HG00741.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-5811dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718975 | ||||||
| chr2:207718975 | TA | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0051 others(5): Show |
8 | HG02015.hp2 HG02486.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-5811delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718975 | ||||||
| chr2:207719028 | G | T | 3 | a0001c0001t0008g0299 a0001c0001t0008g0300 a0001c0005t0001g0298 |
3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.221-5772G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719028 | |||||||
| chr2:207719049 | CAAG | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG00438.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-5750_221-5748d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719049 | |||||||
| chr2:207719302 | C | CT | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.221-5482dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207719302 | ||||||
| chr2:207719302 | C | CTT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0045 others(10): Show |
17 | HG01123.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-5483_221-5482d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207719302 | ||||||
| chr2:207719592 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.221-5208C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719592 | |||||||
| chr2:207719597 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.221-5203G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719597 | |||||||
| chr2:207719749 | G | T | 1 | a0001c0001t0002g0261 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.221-5051G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719749 | |||||||
| chr2:207719775 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0234 |
2 | HG03453.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.221-5025C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719775 | |||||||
| chr2:207720102 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0260 a0001c0001t0002g0269 others(1): Show |
4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-4698C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720102 | |||||||
| chr2:207720107 | C | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.221-4693C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720107 | |||||||
| chr2:207720129 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221-4671A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720129 | |||||||
| chr2:207720171 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
8 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4629G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720171 | |||||||
| chr2:207720187 | C | CA | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.221-4591dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720187 | ||||||
| chr2:207720187 | C | CAA | 42 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0044 others(39): Show |
43 | HG00438.hp1 HG00544.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.221-4592_221-4591d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720187 | ||||||
| chr2:207720211 | G | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0154 |
3 | HG00735.hp1 HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.221-4589G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720211 | |||||||
| chr2:207720288 | T | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0272 a0001c0001t0005g0278 |
4 | HG02145.hp2 HG02280.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-4512T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720288 | |||||||
| chr2:207720298 | C | G | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.221-4502C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720298 | |||||||
| chr2:207720393 | C | CT | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0091 others(5): Show |
8 | HG00597.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4392dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720393 | ||||||
| chr2:207720408 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.221-4392T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720408 | |||||||
| chr2:207720417 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.221-4383T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720417 | |||||||
| chr2:207720558 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0224 |
2 | NA18944.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.221-4242G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720558 | |||||||
| chr2:207720841 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.221-3959C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720841 | |||||||
| chr2:207720892 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-3908C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720892 | |||||||
| chr2:207720901 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-3899G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720901 | |||||||
| chr2:207720961 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-3839G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720961 | |||||||
| chr2:207720978 | G | GT | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.221-3822_221-3821i others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720978 | |||||||
| chr2:207720997 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.221-3803T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720997 | |||||||
| chr2:207721184 | A | C | 1 | a0001c0001t0001g0043 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.221-3616A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721184 | |||||||
| chr2:207721365 | C | T | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.221-3435C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721365 | |||||||
| chr2:207721734 | G | GT | 10 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0194 others(7): Show |
10 | HG01261.hp2 HG01515.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-3052dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207721734 | ||||||
| chr2:207721734 | GT | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
116 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.221-3052delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207721734 | ||||||
| chr2:207721737 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.221-3063T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721737 | |||||||
| chr2:207721911 | T | C | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-2889T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721911 | |||||||
| chr2:207721912 | T | C | 3 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0287 |
3 | NA18966.hp1 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.221-2888T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721912 | |||||||
| chr2:207721916 | T | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(2): Show |
5 | HG00544.hp1 NA18942.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-2884T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721916 | |||||||
| chr2:207721930 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.221-2870C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721930 | |||||||
| chr2:207722073 | A | AT | 89 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(86): Show |
99 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-2710dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | ||||||
| chr2:207722073 | A | ATT | 9 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0181 others(6): Show |
9 | HG00544.hp1 HG01255.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-2711_221-2710d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | ||||||
| chr2:207722073 | AT | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0096 a0001c0001t0001g0100 others(5): Show |
9 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-2710delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | ||||||
| chr2:207722179 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-2621T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722179 | |||||||
| chr2:207722198 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.221-2602G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722198 | |||||||
| chr2:207722203 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.221-2597G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722203 | |||||||
| chr2:207722221 | C | T | 1 | a0001c0001t0017g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.221-2579C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722221 | |||||||
| chr2:207722229 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221-2571C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722229 | |||||||
| chr2:207722402 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-2398A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722402 | |||||||
| chr2:207722457 | C | T | 2 | a0001c0001t0020g0171 a0001c0001t0021g0131 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.221-2343C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722457 | |||||||
| chr2:207722581 | T | G | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-2219T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722581 | |||||||
| chr2:207722848 | A | T | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.221-1952A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722848 | |||||||
| chr2:207722955 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-1845C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722955 | |||||||
| chr2:207722961 | G | GA | 6 | a0001c0001t0001g0100 a0001c0001t0001g0167 a0001c0001t0001g0226 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-1826dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722961 | ||||||
| chr2:207723251 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0222 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.221-1549A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723251 | |||||||
| chr2:207723330 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-1470C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723330 | |||||||
| chr2:207723364 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.221-1436C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723364 | |||||||
| chr2:207723492 | A | G | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-1308A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723492 | |||||||
| chr2:207723695 | G | A | 1 | a0001c0005t0001g0298 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.221-1105G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723695 | |||||||
| chr2:207723829 | C | T | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-971C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723829 | |||||||
| chr2:207723874 | C | CA | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
117 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-905dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207723874 | ||||||
| chr2:207723874 | C | CAA | 8 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0099 others(5): Show |
8 | HG00438.hp1 HG00597.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-906_221-905dup others(2): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207723874 | ||||||
| chr2:207723978 | T | G | 1 | a0001c0001t0009g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.221-822T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723978 | |||||||
| chr2:207724273 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.221-527C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724273 | |||||||
| chr2:207724379 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.221-421A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724379 | |||||||
| chr2:207724469 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-331T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724469 | |||||||
| chr2:207724496 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0137 |
3 | NA19005.hp1 NA19068.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.221-304A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724496 | |||||||
| chr2:207724611 | G | A | 1 | a0001c0001t0013g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.221-189G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724611 | |||||||
| chr2:207724679 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.221-121A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724679 | |||||||
| chr2:207724778 | T | C | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-22T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724778 | |||||||
| chr2:207724926 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0191 |
2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.295+52A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207724926 | |||||||
| chr2:207725126 | A | AT | 113 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0044 others(110): Show |
138 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.295+269dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 207725126 | ||||||
| chr2:207725126 | A | ATT | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(89): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.295+268_295+269dup others(2): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 207725126 | ||||||
| chr2:207725183 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.295+309A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725183 | |||||||
| chr2:207725228 | G | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.295+354G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725228 | |||||||
| chr2:207725232 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.295+358T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725232 | |||||||
| chr2:207725269 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0022g0006 |
3 | HG03225.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.295+395G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725269 | |||||||
| chr2:207725600 | A | G | 1 | a0001c0001t0019g0277 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.295+726A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725600 | |||||||
| chr2:207725737 | A | G | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+863A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725737 | |||||||
| chr2:207725815 | A | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+941A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725815 | |||||||
| chr2:207725825 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.295+951T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725825 | |||||||
| chr2:207725960 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-882A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725960 | |||||||
| chr2:207726144 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.296-698G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726144 | |||||||
| chr2:207726203 | C | A | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-639C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726203 | |||||||
| chr2:207726358 | C | G | 2 | a0001c0001t0007g0145 a0001c0001t0007g0150 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.296-484C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726358 | |||||||
| chr2:207726365 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0221 |
2 | NA18988.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.296-477A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726365 | |||||||
| chr2:207726537 | C | A | 1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.296-305C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726537 | |||||||
| chr2:207726554 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.296-288T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726554 | |||||||
| chr2:207726726 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-116T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726726 | |||||||
| chr2:207726799 | G | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0180 a0001c0001t0001g0198 others(4): Show |
7 | HG01070.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-43G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726799 | |||||||
| chr2:207726978 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+102A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207726978 | |||||||
| chr2:207727042 | G | A | 1 | a0001c0001t0002g0014 | 2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.330+166G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727042 | |||||||
| chr2:207727063 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.330+187A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727063 | |||||||
| chr2:207727322 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.330+446A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727322 | |||||||
| chr2:207727365 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.330+489C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727365 | |||||||
| chr2:207727388 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.330+512G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727388 | |||||||
| chr2:207727439 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.330+563C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727439 | |||||||
| chr2:207727465 | C | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0225 |
4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+589C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727465 | |||||||
| chr2:207727533 | T | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.330+657T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727533 | |||||||
| chr2:207727558 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.330+682A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727558 | |||||||
| chr2:207727706 | TC | T | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+832delC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727706 | ||||||
| chr2:207727880 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+1004A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727880 | |||||||
| chr2:207727952 | TTCTC | T | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1086_330+1089d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727952 | ||||||
| chr2:207727964 | CT | C | 16 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(13): Show |
16 | HG01070.hp1 HG01169.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.330+1104delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727964 | ||||||
| chr2:207728049 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.330+1173T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728049 | |||||||
| chr2:207728183 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+1307C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728183 | |||||||
| chr2:207728206 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.330+1330T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728206 | |||||||
| chr2:207728261 | CT | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
99 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.330+1400delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207728261 | ||||||
| chr2:207728273 | T | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0301 |
2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.330+1397T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728273 | |||||||
| chr2:207728276 | T | A | 1 | a0001c0001t0002g0001 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.330+1400T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728276 | |||||||
| chr2:207728277 | C | A | 1 | a0001c0001t0002g0001 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.330+1401C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728277 | |||||||
| chr2:207728278 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.330+1402T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728278 | |||||||
| chr2:207728428 | A | G | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1552A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728428 | |||||||
| chr2:207728676 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.330+1800A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728676 | |||||||
| chr2:207728765 | G | A | 1 | a0001c0001t0015g0124 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.330+1889G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728765 | |||||||
| chr2:207728808 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.330+1932T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728808 | |||||||
| chr2:207728849 | T | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.330+1973T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728849 | |||||||
| chr2:207728852 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.330+1976A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728852 | |||||||
| chr2:207728858 | G | A | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1982G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728858 | |||||||
| chr2:207728877 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.330+2001A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728877 | |||||||
| chr2:207729044 | G | A | 1 | a0001c0001t0010g0216 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.330+2168G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729044 | |||||||
| chr2:207729052 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.330+2176G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729052 | |||||||
| chr2:207729142 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.330+2266C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729142 | |||||||
| chr2:207729186 | T | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2310T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729186 | |||||||
| chr2:207729201 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.330+2325T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729201 | |||||||
| chr2:207729247 | TCCGCCCC others(17): Show |
T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0093 others(1): Show |
5 | HG01891.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+2374_330+2397d others(26): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729247 | ||||||
| chr2:207729247 | TCCGCCCC others(18): Show |
T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0066 |
4 | HG03139.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+2374_330+2398d others(27): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729247 | ||||||
| chr2:207729248 | CCGCCCCC others(16): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.330+2374_330+2396d others(25): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729248 | ||||||
| chr2:207729250 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.330+2374G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729250 | |||||||
| chr2:207729250 | G | GC | 93 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(90): Show |
101 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.330+2383dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729250 | ||||||
| chr2:207729251 | CCCCCCCC others(13): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0057 |
4 | NA18945.hp2 NA18974.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2384_330+2403d others(22): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729251 | ||||||
| chr2:207729252 | C | A | 6 | a0001c0001t0001g0270 a0001c0001t0002g0001 a0001c0001t0002g0166 others(3): Show |
6 | HG02015.hp1 HG02132.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+2376C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729252 | |||||||
| chr2:207729252 | CCCCCCCC others(12): Show |
C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0082 |
3 | HG03540.hp1 NA19010.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.330+2384_330+2402d others(21): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729252 | ||||||
| chr2:207729252 | CCCCCCCC others(21): Show |
C | 3 | a0001c0001t0001g0221 a0001c0001t0002g0257 a0001c0001t0002g0261 |
3 | NA18961.hp1 NA19074.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.330+2386_330+2413d others(30): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729252 | ||||||
| chr2:207729253 | CCCCCCCG others(11): Show |
C | 1 | a0001c0001t0009g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.330+2384_330+2401d others(20): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729253 | ||||||
| chr2:207729253 | CCCCCCCG others(20): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.330+2384_330+2410d others(29): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729253 | ||||||
| chr2:207729254 | CCCCCCGC others(10): Show |
C | 2 | a0001c0001t0001g0073 a0001c0001t0009g0048 |
2 | HG03139.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.330+2384_330+2400d others(19): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729254 | ||||||
| chr2:207729255 | CCCCCGCC others(4): Show |
C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0037 others(11): Show |
15 | HG00673.hp1 HG01169.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.330+2384_330+2394d others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729255 | ||||||
| chr2:207729255 | CCCCCGCC others(9): Show |
C | 2 | a0001c0001t0001g0112 a0002c0003t0001g0078 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.330+2384_330+2399d others(18): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729255 | ||||||
| chr2:207729256 | CCCCGCCC others(3): Show |
C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0075 others(6): Show |
9 | HG02129.hp2 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+2384_330+2393d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | ||||||
| chr2:207729256 | CCCCGCCC others(8): Show |
C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0071 others(2): Show |
5 | HG00544.hp2 NA18983.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+2384_330+2398d others(17): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | ||||||
| chr2:207729256 | CCCCGCCC others(17): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0107 |
3 | HG01346.hp2 HG02145.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.330+2384_330+2407d others(26): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | ||||||
| chr2:207729257 | CCCGCCCC others(7): Show |
C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0041 others(3): Show |
6 | HG00408.hp1 HG00597.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+2384_330+2397d others(16): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729257 | ||||||
| chr2:207729257 | CCCGCCCC others(16): Show |
C | 1 | a0001c0001t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.330+2384_330+2406d others(25): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729257 | ||||||
| chr2:207729258 | CCGCCCCC others(6): Show |
C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0047 others(7): Show |
12 | HG01069.hp1 HG02071.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.330+2384_330+2396d others(15): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729258 | ||||||
| chr2:207729259 | CGCCCCCA others(5): Show |
C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0043 others(10): Show |
13 | HG01256.hp2 HG02818.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.330+2384_330+2395d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729259 | |||||||
| chr2:207729260 | G | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0077 others(4): Show |
7 | HG02896.hp1 HG03041.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+2384G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729260 | |||||||
| chr2:207729265 | C | G | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.330+2389C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729265 | |||||||
| chr2:207729265 | CACCCCA | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0096 |
3 | NA18956.hp1 NA18956.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.330+2390_330+2395d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729265 | |||||||
| chr2:207729266 | A | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0072 a0001c0001t0001g0099 others(5): Show |
9 | HG00438.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+2390A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729266 | |||||||
| chr2:207729271 | A | AC | 58 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0020 others(55): Show |
62 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.330+2403dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729271 | ||||||
| chr2:207729271 | A | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(36): Show |
42 | HG00438.hp1 HG00673.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.330+2395A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729271 | |||||||
| chr2:207729279 | C | A | 2 | a0001c0001t0003g0273 a0001c0001t0005g0027 |
3 | HG03516.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.330+2403C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729279 | |||||||
| chr2:207729280 | A | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
112 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.330+2404A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729280 | |||||||
| chr2:207729285 | C | G | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+2409C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729285 | |||||||
| chr2:207729288 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0105 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+2412G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729288 | |||||||
| chr2:207729288 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0104 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.330+2412G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729288 | |||||||
| chr2:207729384 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.330+2508A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729384 | |||||||
| chr2:207729386 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.330+2510G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729386 | |||||||
| chr2:207729395 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2519G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729395 | |||||||
| chr2:207729550 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.330+2674C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729550 | |||||||
| chr2:207729550 | C | G | 2 | a0001c0001t0008g0299 a0001c0001t0008g0300 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.330+2674C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729550 | |||||||
| chr2:207729671 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0222 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.330+2795C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729671 | |||||||
| chr2:207729744 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA19064.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.330+2868C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729744 | |||||||
| chr2:207729804 | C | G | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.330+2928C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729804 | |||||||
| chr2:207729814 | C | A | 1 | a0001c0001t0003g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.330+2938C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729814 | |||||||
| chr2:207729882 | AT | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+3019delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729882 | ||||||
| chr2:207729916 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+3040G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729916 | |||||||
| chr2:207729965 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+3089A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729965 | |||||||
| chr2:207730079 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.330+3203G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730079 | |||||||
| chr2:207730215 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.330+3339C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730215 | |||||||
| chr2:207730268 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.330+3392C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730268 | |||||||
| chr2:207730448 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.331-3499T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730448 | |||||||
| chr2:207730480 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.331-3467G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730480 | |||||||
| chr2:207730493 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.331-3454C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730493 | |||||||
| chr2:207730587 | G | A | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-3360G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730587 | |||||||
| chr2:207730733 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.331-3214G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730733 | |||||||
| chr2:207730806 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.331-3141A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730806 | |||||||
| chr2:207730807 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.331-3140C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730807 | |||||||
| chr2:207730906 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.331-3041A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730906 | |||||||
| chr2:207730928 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331-3019C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730928 | |||||||
| chr2:207730955 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0066 others(1): Show |
6 | HG02976.hp2 HG03139.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-2992A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730955 | |||||||
| chr2:207731083 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331-2864A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731083 | |||||||
| chr2:207731243 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.331-2704C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731243 | |||||||
| chr2:207731290 | A | AGGTACTT others(7): Show |
1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.331-2656_331-2643d others(16): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731290 | ||||||
| chr2:207731455 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.331-2492C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731455 | |||||||
| chr2:207731458 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.331-2489A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731458 | |||||||
| chr2:207731718 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.331-2229T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731718 | |||||||
| chr2:207731721 | T | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.331-2226T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731721 | |||||||
| chr2:207731806 | CT | C | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(180): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.331-2120delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | ||||||
| chr2:207731806 | CTT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0087 others(4): Show |
7 | HG01169.hp2 HG01496.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-2121_331-2120d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | ||||||
| chr2:207731806 | CTTT | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
97 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.331-2122_331-2120d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | ||||||
| chr2:207731806 | CTTTT | C | 10 | a0001c0001t0001g0047 a0001c0001t0001g0080 a0001c0001t0001g0092 others(7): Show |
10 | HG01256.hp2 HG02083.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-2123_331-2120d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | ||||||
| chr2:207731840 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.331-2107C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731840 | |||||||
| chr2:207731873 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-2074A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731873 | |||||||
| chr2:207731917 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0228 |
2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.331-2030C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731917 | |||||||
| chr2:207731926 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.331-2021C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731926 | |||||||
| chr2:207731966 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0087 |
2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.331-1981C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731966 | |||||||
| chr2:207732010 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331-1937A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732010 | |||||||
| chr2:207732100 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp1 HG01891.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.331-1847G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732100 | |||||||
| chr2:207732123 | T | C | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-1824T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732123 | |||||||
| chr2:207732263 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.331-1684G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732263 | |||||||
| chr2:207732417 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-1530G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732417 | |||||||
| chr2:207732422 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.331-1525T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732422 | |||||||
| chr2:207732444 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1503G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732444 | |||||||
| chr2:207732594 | G | GT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
112 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.331-1343dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207732594 | ||||||
| chr2:207732636 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.331-1311T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732636 | |||||||
| chr2:207732693 | CCTT | C | 10 | a0001c0001t0002g0125 a0001c0001t0002g0130 a0001c0001t0002g0151 others(7): Show |
10 | HG01099.hp2 HG01168.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.331-1250_331-1248d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207732693 | ||||||
| chr2:207732830 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1117A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732830 | |||||||
| chr2:207732861 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331-1086T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732861 | |||||||
| chr2:207732880 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1067T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732880 | |||||||
| chr2:207732894 | A | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0300 a0001c0005t0001g0298 |
3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.331-1053A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732894 | |||||||
| chr2:207733083 | G | GT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-858dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207733083 | ||||||
| chr2:207733172 | G | A | 1 | a0001c0001t0017g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.331-775G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733172 | |||||||
| chr2:207733266 | C | G | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-681C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733266 | |||||||
| chr2:207733275 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.331-672T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733275 | |||||||
| chr2:207733282 | A | C | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331-665A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733282 | |||||||
| chr2:207733523 | G | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.331-424G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733523 | |||||||
| chr2:207733536 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0225 |
4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-411A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733536 | |||||||
| chr2:207733640 | A | G | 1 | a0001c0004t0002g0008 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-307A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733640 | |||||||
| chr2:207733854 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.331-93T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733854 | |||||||
| chr2:207734118 | G | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0301 |
2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.431+71G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734118 | |||||||
| chr2:207734393 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431+346T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734393 | |||||||
| chr2:207734412 | G | C | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+365G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734412 | |||||||
| chr2:207734579 | CCAA | C | 85 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(82): Show |
110 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.431+541_431+543del others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207734579 | ||||||
| chr2:207734665 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.431+618C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734665 | |||||||
| chr2:207734683 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+636T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734683 | |||||||
| chr2:207734736 | T | C | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.431+689T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734736 | |||||||
| chr2:207734772 | C | CT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
97 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.431+735dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207734772 | ||||||
| chr2:207735274 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.431+1227T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735274 | |||||||
| chr2:207735327 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.431+1280A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735327 | |||||||
| chr2:207735370 | A | T | 10 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0025 others(7): Show |
15 | HG00621.hp1 HG02027.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.431+1323A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735370 | |||||||
| chr2:207735399 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG00438.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+1352C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735399 | |||||||
| chr2:207735498 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+1451A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735498 | |||||||
| chr2:207735499 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+1452T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735499 | |||||||
| chr2:207735727 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.431+1680C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735727 | |||||||
| chr2:207735731 | G | A | 1 | a0001c0001t0018g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.432-1680G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735731 | |||||||
| chr2:207735803 | G | A | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-1608G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735803 | |||||||
| chr2:207735822 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.432-1589C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735822 | |||||||
| chr2:207735874 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.432-1537C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735874 | |||||||
| chr2:207736598 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.432-813T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736598 | |||||||
| chr2:207736621 | C | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-790C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736621 | |||||||
| chr2:207736728 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-683T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736728 | |||||||
| chr2:207736852 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.432-559A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736852 | |||||||
| chr2:207736860 | A | C | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.432-551A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736860 | |||||||
| chr2:207736918 | G | GT | 16 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0001g0077 others(13): Show |
16 | HG01109.hp1 HG01361.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.432-478dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207736918 | ||||||
| chr2:207737018 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.432-393C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737018 | |||||||
| chr2:207737077 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.432-334G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737077 | |||||||
| chr2:207737105 | C | T | 3 | a0001c0001t0002g0297 a0001c0001t0017g0140 a0001c0001t0018g0141 |
3 | HG02615.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.432-306C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737105 | |||||||
| chr2:207737116 | C | T | 77 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(74): Show |
101 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.432-295C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737116 | |||||||
| chr2:207737127 | G | A | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.432-284G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737127 | |||||||
| chr2:207737313 | G | A | 1 | a0001c0002t0001g0293 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.432-98G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737313 | |||||||
| chr2:207737381 | G | A | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-30G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737381 | |||||||
| chr2:207737386 | AAATAATT others(9): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.432-24_432-9delAAT others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737386 | |||||||
| chr2:207737507 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.467+61C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737507 | |||||||
| chr2:207737599 | G | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0170 |
3 | HG02735.hp2 HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.467+153G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737599 | |||||||
| chr2:207737690 | A | AT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
100 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.467+247dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737690 | ||||||
| chr2:207737693 | T | TA | 22 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0106 others(19): Show |
24 | HG00597.hp2 HG01243.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.467+258dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737693 | ||||||
| chr2:207737693 | TA | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0203 others(9): Show |
16 | HG00609.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.467+258delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737693 | ||||||
| chr2:207737861 | T | A | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.467+415T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737861 | |||||||
| chr2:207737865 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.467+419C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737865 | |||||||
| chr2:207737901 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+455C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737901 | |||||||
| chr2:207738042 | A | G | 2 | a0001c0001t0002g0256 a0001c0001t0002g0286 |
2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.467+596A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738042 | |||||||
| chr2:207738182 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.467+736C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738182 | |||||||
| chr2:207738231 | G | GT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(96): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.467+793dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207738231 | ||||||
| chr2:207738231 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.467+785G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738231 | |||||||
| chr2:207738346 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+900G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738346 | |||||||
| chr2:207738449 | G | A | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.467+1003G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738449 | |||||||
| chr2:207738594 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+1148T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738594 | |||||||
| chr2:207738714 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+1268C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738714 | |||||||
| chr2:207739225 | T | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-1430T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739225 | |||||||
| chr2:207739273 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.468-1382C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739273 | |||||||
| chr2:207739538 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.468-1117C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739538 | |||||||
| chr2:207739653 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.468-1002C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739653 | |||||||
| chr2:207739673 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468-982T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739673 | |||||||
| chr2:207739872 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-783G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739872 | |||||||
| chr2:207739939 | T | G | 1 | a0001c0001t0018g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.468-716T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739939 | |||||||
| chr2:207739941 | C | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-714C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739941 | |||||||
| chr2:207739951 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-704A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739951 | |||||||
| chr2:207740075 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-580C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740075 | |||||||
| chr2:207740084 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-571G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740084 | |||||||
| chr2:207740173 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.468-482A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740173 | |||||||
| chr2:207740202 | A | T | 1 | a0001c0001t0012g0172 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.468-453A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740202 | |||||||
| chr2:207740470 | G | A | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.468-185G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740470 | |||||||
| chr2:207740577 | G | GC | 4 | a0001c0001t0002g0147 a0001c0001t0002g0260 a0001c0001t0002g0269 others(1): Show |
4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-76dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207740577 | ||||||
| chr2:207740768 | G | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.519+62G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740768 | |||||||
| chr2:207740840 | T | C | 3 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 |
3 | NA18944.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.519+134T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740840 | |||||||
| chr2:207740870 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.519+164T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740870 | |||||||
| chr2:207741147 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
114 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.519+441T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741147 | |||||||
| chr2:207741252 | CA | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.519+558delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207741252 | ||||||
| chr2:207741259 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.519+553A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741259 | |||||||
| chr2:207741264 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.519+558A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741264 | |||||||
| chr2:207741271 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0045 others(4): Show |
10 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+565A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741271 | |||||||
| chr2:207741359 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(89): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.519+653A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741359 | |||||||
| chr2:207741444 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.519+738A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741444 | |||||||
| chr2:207741651 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(2): Show |
6 | NA18954.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-572C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741651 | |||||||
| chr2:207741710 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-513T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741710 | |||||||
| chr2:207741833 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-390A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741833 | |||||||
| chr2:207741843 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0201 a0001c0001t0001g0228 |
3 | HG01109.hp1 HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.520-380C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741843 | |||||||
| chr2:207741845 | CA | C | 14 | a0001c0001t0001g0253 a0001c0001t0001g0302 a0001c0001t0002g0143 others(11): Show |
15 | HG01168.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-362delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207741845 | ||||||
| chr2:207741873 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.520-350G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741873 | |||||||
| chr2:207741890 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-333C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741890 | |||||||
| chr2:207741927 | G | A | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-296G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741927 | |||||||
| chr2:207742151 | C | CA | 6 | a0001c0001t0002g0122 a0001c0001t0002g0142 a0001c0001t0002g0143 others(3): Show |
6 | HG01243.hp1 HG02015.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-55dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | ||||||
| chr2:207742151 | CA | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0253 others(3): Show |
6 | HG03486.hp2 HG03942.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-55delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | ||||||
| chr2:207742151 | CAA | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(88): Show |
106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.520-56_520-55delAA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | ||||||
| chr2:207742421 | A | G | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.639+79A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742421 | |||||||
| chr2:207742480 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.639+138C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742480 | |||||||
| chr2:207742552 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.639+210A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742552 | |||||||
| chr2:207742712 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.639+370G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742712 | |||||||
| chr2:207742752 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.639+410C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742752 | |||||||
| chr2:207743123 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.639+781G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743123 | |||||||
| chr2:207743141 | T | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0261 |
2 | NA18961.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.639+799T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743141 | |||||||
| chr2:207743538 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.639+1196G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743538 | |||||||
| chr2:207743576 | C | T | 2 | a0001c0001t0017g0140 a0001c0001t0018g0141 |
2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.639+1234C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743576 | |||||||
| chr2:207743720 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.639+1378G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743720 | |||||||
| chr2:207743763 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.639+1421C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743763 | |||||||
| chr2:207743769 | A | T | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.639+1427A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743769 | |||||||
| chr2:207743806 | T | TTTTTTG | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(88): Show |
106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.639+1487_639+1492d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | ||||||
| chr2:207743806 | T | TTTTTTGT others(5): Show |
1 | a0001c0001t0001g0041 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.639+1481_639+1492d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | ||||||
| chr2:207743806 | TTTTTTGT others(5): Show |
T | 1 | a0001c0001t0002g0012 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639+1481_639+1492d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | ||||||
| chr2:207743812 | G | T | 1 | a0001c0001t0002g0261 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.639+1470G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743812 | |||||||
| chr2:207743912 | C | G | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.639+1570C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743912 | |||||||
| chr2:207743915 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(5): Show |
8 | HG01069.hp1 HG02486.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+1573G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743915 | |||||||
| chr2:207744053 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0232 |
2 | NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.639+1711A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744053 | |||||||
| chr2:207744065 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.639+1723A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744065 | |||||||
| chr2:207744080 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.639+1738G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744080 | |||||||
| chr2:207744092 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(43): Show |
53 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.639+1750T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744092 | |||||||
| chr2:207744095 | C | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(103): Show |
123 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.639+1753C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744095 | |||||||
| chr2:207744117 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.639+1775G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744117 | |||||||
| chr2:207744218 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.639+1876C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744218 | |||||||
| chr2:207744228 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.639+1886T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744228 | |||||||
| chr2:207744228 | T | TTG | 10 | a0001c0001t0001g0070 a0001c0001t0001g0134 a0001c0001t0001g0180 others(7): Show |
10 | HG01070.hp2 HG01081.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.639+1906_639+1907d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | ||||||
| chr2:207744228 | T | TTGTGTG | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0118 others(4): Show |
7 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+1902_639+1907d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | ||||||
| chr2:207744228 | T | TTGTGTGT others(1): Show |
83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
98 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.639+1900_639+1907d others(10): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | ||||||
| chr2:207744228 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0083 a0001c0001t0001g0113 a0001c0001t0013g0074 |
3 | HG00408.hp1 HG04115.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.639+1898_639+1907d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | ||||||
| chr2:207744295 | G | C | 1 | a0001c0005t0001g0298 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.639+1953G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744295 | |||||||
| chr2:207744326 | G | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.639+1984G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744326 | |||||||
| chr2:207744401 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.639+2059A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744401 | |||||||
| chr2:207744530 | A | AT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
117 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.639+2206dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744530 | ||||||
| chr2:207744600 | C | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(97): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.639+2258C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744600 | |||||||
| chr2:207744612 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(94): Show |
106 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.639+2270C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744612 | |||||||
| chr2:207744940 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(2): Show |
6 | NA18954.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-2107A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744940 | |||||||
| chr2:207745072 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0111 |
2 | NA18973.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.640-1975C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745072 | |||||||
| chr2:207745265 | G | A | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-1782G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745265 | |||||||
| chr2:207745331 | G | C | 4 | a0001c0001t0002g0122 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | HG01243.hp1 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1716G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745331 | |||||||
| chr2:207745408 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.640-1639C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745408 | |||||||
| chr2:207745475 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-1572G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745475 | |||||||
| chr2:207745810 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1237G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745810 | |||||||
| chr2:207746077 | A | G | 86 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(83): Show |
111 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.640-970A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746077 | |||||||
| chr2:207746128 | C | T | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.640-919C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746128 | |||||||
| chr2:207746216 | T | C | 1 | a0001c0001t0010g0216 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.640-831T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746216 | |||||||
| chr2:207746278 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.640-769A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746278 | |||||||
| chr2:207746294 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-753C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746294 | |||||||
| chr2:207746361 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-686G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746361 | |||||||
| chr2:207746553 | G | A | 80 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0001g0250 others(77): Show |
104 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.640-494G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746553 | |||||||
| chr2:207746584 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.640-463T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746584 | |||||||
| chr2:207746663 | T | C | 92 | a0001c0001t0001g0024 a0001c0001t0001g0176 a0001c0001t0001g0179 others(89): Show |
117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.640-384T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746663 | |||||||
| chr2:207746717 | C | T | 3 | a0001c0001t0007g0144 a0001c0001t0007g0145 a0001c0001t0007g0150 |
3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640-330C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746717 | |||||||
| chr2:207746899 | C | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.640-148C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746899 | |||||||
| chr2:207746962 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.640-85T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746962 | |||||||
| chr2:207746971 | G | A | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-76G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746971 | |||||||
| chr2:207746975 | C | CA | 16 | a0001c0001t0001g0031 a0001c0001t0001g0133 a0001c0001t0001g0221 others(13): Show |
18 | HG00738.hp1 HG00738.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.640-57dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207746975 | ||||||
| chr2:207747307 | A | G | 1 | a0001c0001t0012g0172 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.806+94A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747307 | |||||||
| chr2:207747358 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.806+145A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747358 | |||||||
| chr2:207747501 | TTACAAG | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+291_806+296del others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 207747501 | ||||||
| chr2:207747506 | A | G | 1 | a0001c0001t0007g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.806+293A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747506 | |||||||
| chr2:207747602 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+389G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747602 | |||||||
| chr2:207747801 | G | T | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+588G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747801 | |||||||
| chr2:207747811 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.806+598G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747811 | |||||||
| chr2:207747907 | T | TTTCA | 4 | a0001c0001t0002g0012 a0001c0001t0005g0027 a0001c0001t0005g0272 others(1): Show |
6 | HG02145.hp2 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+717_806+720dup others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 207747907 | ||||||
| chr2:207747981 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.806+768A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747981 | |||||||
| chr2:207748076 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.806+863T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748076 | |||||||
| chr2:207748211 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+998C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748211 | |||||||
| chr2:207748243 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.806+1030C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748243 | |||||||
| chr2:207748289 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0264 |
2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.806+1076C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748289 | |||||||
| chr2:207748290 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0225 |
4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+1077G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748290 | |||||||
| chr2:207748379 | G | A | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+1166G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748379 | |||||||
| chr2:207748455 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+1242T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748455 | |||||||
| chr2:207748466 | G | A | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.806+1253G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748466 | |||||||
| chr2:207748512 | T | G | 1 | a0001c0001t0003g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.806+1299T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748512 | |||||||
| chr2:207748603 | T | A | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806+1390T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748603 | |||||||
| chr2:207748770 | C | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.806+1557C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748770 | |||||||
| chr2:207748783 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.806+1570T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748783 | |||||||
| chr2:207748794 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.806+1581T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748794 | |||||||
| chr2:207748799 | C | G | 1 | a0001c0001t0008g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806+1586C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748799 | |||||||
| chr2:207748905 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+1692G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748905 | |||||||
| chr2:207748926 | A | G | 1 | a0001c0001t0002g0023 | 2 | NA19007.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.806+1713A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748926 | |||||||
| chr2:207748926 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.806+1713A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748926 | |||||||
| chr2:207748983 | A | G | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.806+1770A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748983 | |||||||
| chr2:207749022 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(74): Show |
89 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.806+1809C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749022 | |||||||
| chr2:207749030 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.806+1817C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749030 | |||||||
| chr2:207749345 | G | A | 1 | a0001c0001t0018g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-1612G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749345 | |||||||
| chr2:207749447 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1510C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749447 | |||||||
| chr2:207749502 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-1455A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749502 | |||||||
| chr2:207749529 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.807-1428C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749529 | |||||||
| chr2:207749547 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.807-1410T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749547 | |||||||
| chr2:207749572 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.807-1385T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749572 | |||||||
| chr2:207749842 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0009g0048 others(5): Show |
8 | HG01069.hp1 HG02486.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-1115G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749842 | |||||||
| chr2:207749891 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(86): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.807-1066T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749891 | |||||||
| chr2:207749954 | A | C | 1 | a0001c0001t0002g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.807-1003A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749954 | |||||||
| chr2:207750075 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-882T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750075 | |||||||
| chr2:207750079 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-878A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750079 | |||||||
| chr2:207750101 | G | A | 3 | a0001c0002t0001g0292 a0001c0002t0001g0294 a0001c0002t0001g0295 |
3 | HG01069.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.807-856G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750101 | |||||||
| chr2:207750267 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-690G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750267 | |||||||
| chr2:207750354 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.807-603C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750354 | |||||||
| chr2:207750656 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(2): Show |
5 | HG00544.hp1 NA18942.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-301G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750656 | |||||||
| chr2:207750661 | G | T | 1 | a0001c0001t0021g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.807-296G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750661 | |||||||
| chr2:207750800 | T | G | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(1): Show |
4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-157T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750800 | |||||||
| chr2:207750813 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-144C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750813 | |||||||
| chr2:207751138 | T | G | 1 | a0001c0001t0002g0288 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.969+19T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751138 | |||||||
| chr2:207751322 | A | C | 89 | a0001c0001t0001g0024 a0001c0001t0001g0176 a0001c0001t0001g0179 others(86): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.969+203A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751322 | |||||||
| chr2:207751573 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.969+454G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751573 | |||||||
| chr2:207751580 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.969+461C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751580 | |||||||
| chr2:207751581 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.969+462G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751581 | |||||||
| chr2:207751593 | G | A | 1 | a0001c0001t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.969+474G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751593 | |||||||
| chr2:207751621 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+502G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751621 | |||||||
| chr2:207751637 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.969+518C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751637 | |||||||
| chr2:207751704 | A | G | 1 | a0001c0001t0018g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.969+585A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751704 | |||||||
| chr2:207751809 | G | A | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(189): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.969+690G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751809 | |||||||
| chr2:207751841 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0260 a0001c0001t0002g0269 others(1): Show |
4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+722C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751841 | |||||||
| chr2:207751854 | CAAAA | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0138 others(21): Show |
29 | HG00597.hp1 HG00609.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.969+749_969+752del others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207751854 | ||||||
| chr2:207751945 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+826G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751945 | |||||||
| chr2:207751967 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+848G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751967 | |||||||
| chr2:207751976 | A | G | 1 | a0001c0001t0020g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.969+857A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751976 | |||||||
| chr2:207751995 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0291 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.969+876G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751995 | |||||||
| chr2:207752082 | A | G | 10 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 others(7): Show |
11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.969+963A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752082 | |||||||
| chr2:207752121 | A | ATT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+1002_969+1003i others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752121 | |||||||
| chr2:207752224 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+1105G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752224 | |||||||
| chr2:207752351 | T | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.969+1232T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752351 | |||||||
| chr2:207752392 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.970-1196A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752392 | |||||||
| chr2:207752437 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.970-1151G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752437 | |||||||
| chr2:207752442 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.970-1146G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752442 | |||||||
| chr2:207752534 | C | CA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.970-1041dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752534 | ||||||
| chr2:207752534 | C | CAA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | HG02074.hp1 HG03831.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.970-1042_970-1041d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752534 | ||||||
| chr2:207752548 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.970-1040T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752548 | |||||||
| chr2:207752758 | G | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(65): Show |
76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.970-830G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752758 | |||||||
| chr2:207752803 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.970-785G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752803 | |||||||
| chr2:207752811 | CG | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.970-774delG | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752811 | ||||||
| chr2:207752812 | G | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0136 a0001c0001t0001g0137 others(14): Show |
18 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.970-776G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752812 | |||||||
| chr2:207752914 | C | CTGT | 84 | a0001c0001t0001g0024 a0001c0001t0001g0176 a0001c0001t0001g0179 others(81): Show |
108 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.970-673_970-671dup others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752914 | ||||||
| chr2:207752974 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.970-614G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752974 | |||||||
| chr2:207752981 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.970-607A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752981 | |||||||
| chr2:207753027 | C | CA | 6 | a0001c0001t0006g0054 a0001c0001t0020g0171 a0001c0002t0001g0292 others(3): Show |
6 | HG01069.hp1 HG01884.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-549dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207753027 | ||||||
| chr2:207753076 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.970-512C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753076 | |||||||
| chr2:207753245 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.970-343C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753245 | |||||||
| chr2:207753468 | T | C | 1 | a0001c0001t0002g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.970-120T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753468 | |||||||
| chr2:207753501 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.970-87C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753501 | |||||||
| chr2:207753537 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.970-51G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753537 |