Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 904 |
| ensemblid | ENSG00000129315.12 |
| hgncid | 1599 |
| symbol | CCNT1 |
| name | cyclin T1 |
| refseq_nuc | NM_001240.4 |
| refseq_prot | NP_001231.2 |
| ensembl_nuc | ENST00000261900.8 |
| ensembl_prot | ENSP00000261900.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48688458 |
| end | 48716707 |
| strand | - |
| ver | v1.2 |
| region | chr12:48688458-48716707 |
| region5000 | chr12:48683458-48721707 |
| regionname0 | CCNT1_chr12_48688458_48716707 |
| regionname5000 | CCNT1_chr12_48683458_48721707 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 726 | 377 | 92 | 67 | 166 | 14 | 36 | 128 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| a0002 | 0/0 | 726 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| a0003 | 0/0 | 726 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| a0004 | 0/0 | 726 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| a0005 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| a0006 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | MEGER others(721): Show |
chr12 | 48683458 | 48721707 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2178 | 203 | 33 | 32 | 119 | 5 | 14 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0001c0002 | 1/1 | 2178 | 145 | 50 | 27 | 47 | 4 | 15 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0001c0003 | 0/0 | 2178 | 28 | 8 | 8 | 0 | 5 | 7 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0001c0009 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0002c0004 | 0/0 | 2178 | 3 | 2 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0003c0006 | 0/0 | 2178 | 2 | 0 | 2 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0004c0005 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0005c0008 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 | ||
| a0006c0007 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | ATGGA others(2173): Show |
chr12 | 48683458 | 48721707 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6789 | 121 | 20 | 12 | 78 | 1 | 10 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0004 | 0/0 | 6787 | 17 | 1 | 0 | 15 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6782): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0005 | 0/0 | 6789 | 14 | 0 | 9 | 5 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0006 | 0/0 | 6789 | 12 | 0 | 2 | 8 | 0 | 2 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0007 | 0/0 | 6789 | 12 | 1 | 7 | 0 | 4 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0008 | 0/0 | 6788 | 7 | 7 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0009 | 0/0 | 6785 | 7 | 0 | 0 | 7 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6780): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0013 | 0/0 | 6789 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0014 | 0/0 | 6784 | 3 | 2 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6779): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0015 | 0/0 | 6789 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0019 | 0/0 | 6789 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0021 | 0/0 | 6784 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6779): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0028 | 0/0 | 6789 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0031 | 0/0 | 6789 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0001t0033 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0002 | 1/1 | 6788 | 120 | 32 | 25 | 46 | 3 | 12 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0003 | 0/0 | 6788 | 6 | 6 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0011 | 0/0 | 6788 | 5 | 4 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0016 | 0/0 | 6788 | 2 | 0 | 0 | 0 | 0 | 2 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0017 | 0/0 | 6788 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0018 | 0/0 | 6788 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0020 | 0/0 | 6788 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0022 | 0/0 | 6788 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0023 | 0/0 | 6788 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0024 | 0/0 | 6789 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0026 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0027 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0030 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0002t0032 | 0/0 | 6788 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0003t0003 | 0/0 | 6788 | 21 | 2 | 7 | 0 | 5 | 7 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0003t0010 | 0/0 | 6788 | 6 | 6 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0003t0029 | 0/0 | 6788 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0001c0009t0003 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0002c0004t0012 | 0/0 | 6788 | 3 | 2 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0003c0006t0002 | 0/0 | 6788 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0003c0006t0025 | 0/0 | 6788 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0004c0005t0001 | 0/0 | 6789 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6784): Show |
chr12 | 48683458 | 48721707 |
| a0005c0008t0012 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| a0006c0007t0008 | 0/0 | 6788 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | AGCCT others(6783): Show |
chr12 | 48683458 | 48721707 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 5 | 15 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 2 | 0 | 0 | 5 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0006 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0008 | 0/0 | 8 | 0 | 7 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0007g0004 | 0/0 | 10 | 1 | 6 | 0 | 3 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0013g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0013g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0014g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0015g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0019g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0028g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0031g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0001t0033g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0002 | 0/0 | 16 | 1 | 1 | 13 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0003 | 0/0 | 12 | 0 | 9 | 0 | 1 | 2 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0007 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0010 | 0/0 | 7 | 1 | 3 | 0 | 0 | 3 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0016g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0017g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0018g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0020g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0022g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0023g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0024g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0026g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0027g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0030g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0002t0032g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0009 | 0/0 | 8 | 1 | 4 | 0 | 0 | 3 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0010g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0003t0029g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0001c0009t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0002c0004t0012g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0003c0006t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0003c0006t0025g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0004c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0004c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0005c0008t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| a0006c0007t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0032 | g0117 | EUR | GBR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0215 | EUR | GBR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0039 | EUR | FIN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0146 | EUR | FIN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00639 | hp1 | a0001 | c0001 | t0019 | g0178 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00738 | hp2 | a0001 | c0002 | t0022 | g0125 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01109 | hp2 | a0002 | c0004 | t0012 | g0022 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01167 | hp1 | a0001 | c0002 | t0011 | g0053 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01167 | hp2 | a0003 | c0006 | t0025 | g0068 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01169 | hp1 | a0003 | c0006 | t0002 | g0067 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0222 | AMR | PUR | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01255 | hp1 | a0001 | c0003 | t0029 | g0213 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0218 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0009 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0057 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0147 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0219 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01515 | hp1 | a0001 | c0003 | t0003 | g0220 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0090 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0217 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0004 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0091 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01517 | hp2 | a0001 | c0003 | t0003 | g0216 | EUR | IBS | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01884 | hp2 | a0001 | c0001 | t0033 | g0062 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02015 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02055 | hp1 | a0001 | c0002 | t0027 | g0052 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02083 | hp1 | a0001 | c0001 | t0031 | g0158 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0169 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02155 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | CDX | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0099 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02258 | hp1 | a0002 | c0004 | t0012 | g0022 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | KHV | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02572 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02602 | hp1 | a0001 | c0002 | t0016 | g0103 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02602 | hp2 | a0001 | c0002 | t0016 | g0109 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02615 | hp1 | a0001 | c0003 | t0010 | g0040 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0106 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02630 | hp1 | a0001 | c0002 | t0011 | g0019 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02630 | hp2 | a0001 | c0002 | t0030 | g0100 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02683 | hp1 | a0001 | c0002 | t0020 | g0082 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02717 | hp2 | a0001 | c0003 | t0010 | g0226 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02723 | hp1 | a0002 | c0004 | t0012 | g0022 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0221 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0060 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0058 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02809 | hp2 | a0001 | c0003 | t0010 | g0225 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02818 | hp1 | a0001 | c0003 | t0010 | g0040 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0075 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0056 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02922 | hp2 | a0001 | c0003 | t0010 | g0223 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02970 | hp2 | a0001 | c0002 | t0018 | g0098 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0095 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0077 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03195 | hp2 | a0001 | c0002 | t0011 | g0041 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0101 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03209 | hp2 | a0001 | c0002 | t0017 | g0029 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03225 | hp1 | a0001 | c0002 | t0026 | g0054 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03453 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0180 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0214 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | ESN | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03540 | hp1 | a0001 | c0003 | t0010 | g0224 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03579 | hp2 | a0001 | c0002 | t0024 | g0108 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0212 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0009 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0085 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0009 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0009 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04184 | hp2 | a0001 | c0003 | t0003 | g0039 | SAS | BEB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04204 | hp2 | a0001 | c0001 | t0028 | g0165 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0154 | SAS | STU | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18522 | hp2 | a0001 | c0002 | t0018 | g0097 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | CHB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18945 | hp2 | a0001 | c0001 | t0013 | g0033 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18949 | hp1 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18980 | hp2 | a0001 | c0002 | t0023 | g0105 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18983 | hp1 | a0004 | c0005 | t0001 | g0140 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18988 | hp2 | a0001 | c0001 | t0013 | g0033 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19000 | hp1 | a0001 | c0001 | t0015 | g0166 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19007 | hp2 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19060 | hp1 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19068 | hp1 | a0004 | c0005 | t0001 | g0210 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19082 | hp2 | a0001 | c0001 | t0013 | g0138 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19091 | hp2 | a0001 | c0001 | t0015 | g0164 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | YRI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | ASW | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20129 | hp2 | a0001 | c0002 | t0017 | g0029 | AFR | ASW | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | TSI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0004 | EUR | TSI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0004 | EUR | TSI | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | GIH | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02109 | hp1 | a0005 | c0008 | t0012 | g0136 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0055 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0137 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG06807 | hp1 | a0006 | c0007 | t0008 | g0074 | AFR | USA | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0076 | AFR | USA | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | USA | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | USA | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA21309 | hp1 | a0001 | c0009 | t0003 | g0133 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | LWK | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0079 | REF | REF | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0081 | REF | REF | CCNT1_chr12_48683458_48721707 | CCNT1 | chr12 | 48683458 | 48721707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48693244 | T | C | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1970A>G | p.Tyr657Cys | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2002/6788 | 1970/2181 | 657/726 | chr12 | 48693244 | |||
| chr12:48693304 | G | A | 1 | a0006 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1910C>T | p.Ser637Leu | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1942/6788 | 1910/2181 | 637/726 | chr12 | 48693304 | |||
| chr12:48693488 | G | T | 1 | a0004 | 2 | NA18983.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.1726C>A | p.Pro576Thr | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1758/6788 | 1726/2181 | 576/726 | chr12 | 48693488 | |||
| chr12:48693748 | G | A | 1 | a0003 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.1466C>T | p.Ala489Val | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1498/6788 | 1466/2181 | 489/726 | chr12 | 48693748 | |||
| chr12:48694129 | T | C | 2 | a0002 a0005 |
4 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
missense_variant | MODERATE | c.1085A>G | p.His362Arg | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1117/6788 | 1085/2181 | 362/726 | chr12 | 48694129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48693180 | G | A | 6 | a0001c0001 a0001c0003 a0002c0004 others(3): Show |
238 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(235): Show |
synonymous_variant | LOW | c.2034C>T | p.Pro678Pro | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2066/6788 | 2034/2181 | 678/726 | chr12 | 48693180 | |||
| chr12:48693873 | G | C | 1 | a0001c0003 | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
synonymous_variant | LOW | c.1341C>G | p.Pro447Pro | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1373/6788 | 1341/2181 | 447/726 | chr12 | 48693873 | |||
| chr12:48694185 | T | C | 1 | a0001c0009 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1029A>G | p.Leu343Leu | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1061/6788 | 1029/2181 | 343/726 | chr12 | 48694185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48688486 | T | C | 1 | a0003c0006t0025 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4547A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4547 | chr12 | 48688486 | ||||||
| chr12:48688487 | G | A | 1 | a0001c0002t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4546C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4546 | chr12 | 48688487 | ||||||
| chr12:48688618 | C | T | 1 | a0001c0003t0029 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4415G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4415 | chr12 | 48688618 | ||||||
| chr12:48688682 | C | A | 1 | a0001c0002t0011 | 5 | HG01167.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4351G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4351 | chr12 | 48688682 | ||||||
| chr12:48688700 | C | T | 2 | a0001c0001t0006 a0001c0001t0031 |
13 | HG01081.hp2 HG01928.hp2 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4333G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4333 | chr12 | 48688700 | ||||||
| chr12:48688788 | G | A | 1 | a0001c0002t0027 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4245C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4245 | chr12 | 48688788 | ||||||
| chr12:48688788 | GAC | G | 1 | a0001c0001t0009 | 7 | HG02015.hp2 HG02080.hp1 HG02132.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4243_*4244delGT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4243 | chr12 | 48688788 | ||||||
| chr12:48688810 | C | CT | 13 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(10): Show |
194 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*4222dupA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4222 | chr12 | 48688810 | ||||||
| chr12:48688844 | GAA | G | 2 | a0001c0001t0004 a0001c0001t0009 |
24 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4187_*4188delTT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4187 | chr12 | 48688844 | ||||||
| chr12:48688847 | A | G | 1 | a0001c0002t0016 | 2 | HG02602.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4186T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4186 | chr12 | 48688847 | ||||||
| chr12:48688871 | G | A | 1 | a0001c0002t0030 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4162C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4162 | chr12 | 48688871 | ||||||
| chr12:48689031 | A | T | 1 | a0001c0002t0023 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4002T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 4002 | chr12 | 48689031 | ||||||
| chr12:48689048 | T | C | 1 | a0001c0002t0018 | 2 | HG02970.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3985A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 3985 | chr12 | 48689048 | ||||||
| chr12:48689488 | G | A | 1 | a0001c0001t0007 | 12 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3545C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 3545 | chr12 | 48689488 | ||||||
| chr12:48689611 | G | T | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(18): Show |
235 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*3422C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 3422 | chr12 | 48689611 | ||||||
| chr12:48689670 | T | C | 1 | a0001c0001t0031 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3363A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 3363 | chr12 | 48689670 | ||||||
| chr12:48690211 | G | T | 1 | a0001c0003t0010 | 6 | HG02615.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2822C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2822 | chr12 | 48690211 | ||||||
| chr12:48690613 | C | T | 1 | a0001c0001t0028 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2420G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2420 | chr12 | 48690613 | ||||||
| chr12:48690643 | C | A | 1 | a0001c0002t0017 | 2 | HG03209.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2390G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2390 | chr12 | 48690643 | ||||||
| chr12:48690651 | G | A | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(23): Show |
248 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 2382 | chr12 | 48690651 | ||||||
| chr12:48691282 | T | C | 1 | a0001c0002t0032 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1751A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1751 | chr12 | 48691282 | ||||||
| chr12:48691399 | T | C | 1 | a0001c0001t0033 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1634 | chr12 | 48691399 | ||||||
| chr12:48691475 | T | C | 1 | a0001c0001t0014 | 3 | HG01346.hp2 HG02809.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1558A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1558 | chr12 | 48691475 | ||||||
| chr12:48691531 | G | T | 1 | a0001c0001t0005 | 14 | HG00733.hp1 HG01071.hp1 HG01109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1502C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1502 | chr12 | 48691531 | ||||||
| chr12:48691872 | A | C | 1 | a0001c0001t0015 | 2 | NA19000.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1161T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1161 | chr12 | 48691872 | ||||||
| chr12:48691902 | A | C | 1 | a0001c0002t0022 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1131 | chr12 | 48691902 | ||||||
| chr12:48691989 | T | C | 2 | a0002c0004t0012 a0005c0008t0012 |
4 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1044A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 1044 | chr12 | 48691989 | ||||||
| chr12:48692390 | TTACA | T | 2 | a0001c0001t0014 a0001c0001t0021 |
4 | HG01346.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*639_*642delTGTA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 639 | chr12 | 48692390 | ||||||
| chr12:48692401 | C | T | 1 | a0001c0002t0020 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*632G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 632 | chr12 | 48692401 | ||||||
| chr12:48692665 | A | T | 1 | a0001c0001t0013 | 3 | NA18945.hp2 NA18988.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 368 | chr12 | 48692665 | ||||||
| chr12:48692758 | G | T | 1 | a0001c0001t0019 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 9/9 | 275 | chr12 | 48692758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48694723 | T | C | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-287A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48694723 | |||||||
| chr12:48694724 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.778-288T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48694724 | |||||||
| chr12:48695012 | C | T | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-576G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48695012 | |||||||
| chr12:48695061 | T | C | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-625A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48695061 | |||||||
| chr12:48695191 | G | A | 1 | a0001c0002t0002g0110 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.777+568C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48695191 | |||||||
| chr12:48695413 | G | A | 2 | a0001c0002t0002g0083 a0001c0002t0002g0088 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.777+346C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48695413 | |||||||
| chr12:48695652 | A | G | 1 | a0001c0002t0002g0066 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.777+107T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 8/8 | chr12 | 48695652 | |||||||
| chr12:48696239 | T | TA | 16 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(13): Show |
20 | HG01071.hp2 HG01192.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.543-78dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696239 | |||||||
| chr12:48696239 | TA | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(116): Show |
248 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.543-78delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696239 | |||||||
| chr12:48696239 | TAA | T | 27 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0163 others(24): Show |
27 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.543-79_543-78delTT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696239 | |||||||
| chr12:48696240 | A | T | 1 | a0001c0002t0002g0003 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.543-78T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696240 | |||||||
| chr12:48696241 | A | T | 3 | a0001c0001t0001g0172 a0001c0001t0004g0167 a0001c0002t0002g0123 |
3 | NA18948.hp1 NA18950.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.543-79T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696241 | |||||||
| chr12:48696417 | G | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
7 | HG00544.hp2 HG02015.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-255C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696417 | |||||||
| chr12:48696421 | CA | C | 9 | a0001c0001t0001g0161 a0001c0002t0003g0016 a0001c0002t0003g0099 others(6): Show |
12 | HG01257.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.543-260delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696421 | |||||||
| chr12:48696894 | G | A | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-732C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696894 | |||||||
| chr12:48696943 | G | A | 1 | a0001c0001t0007g0004 | 10 | HG00642.hp1 HG01081.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-781C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48696943 | |||||||
| chr12:48697049 | G | T | 1 | a0001c0001t0005g0194 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.543-887C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697049 | |||||||
| chr12:48697064 | C | T | 6 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(3): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.543-902G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697064 | |||||||
| chr12:48697189 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(52): Show |
108 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.542+949A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697189 | |||||||
| chr12:48697279 | G | A | 1 | a0001c0003t0003g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.542+859C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697279 | |||||||
| chr12:48697390 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0001g0187 others(1): Show |
4 | HG02129.hp1 NA18950.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+748G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697390 | |||||||
| chr12:48697522 | T | TA | 18 | a0001c0001t0001g0145 a0001c0002t0002g0069 a0001c0002t0002g0070 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.542+615dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697522 | |||||||
| chr12:48697522 | T | TAAAAAA | 3 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+610_542+615dup others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697522 | |||||||
| chr12:48697522 | T | TAAAAAAA others(4): Show |
1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.542+605_542+615dup others(11): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697522 | |||||||
| chr12:48697522 | T | TAAAAAAA others(6): Show |
1 | a0001c0002t0018g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542+603_542+615dup others(13): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697522 | |||||||
| chr12:48697523 | A | T | 1 | a0001c0001t0009g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.542+615T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697523 | |||||||
| chr12:48697532 | A | T | 1 | a0001c0002t0027g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.542+606T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697532 | |||||||
| chr12:48697534 | A | AAAAAAAA others(38): Show |
1 | a0001c0002t0018g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.542+603_542+604ins others(45): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697534 | A | AAAAAAAA others(10): Show |
1 | a0001c0002t0030g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.542+603_542+604ins others(17): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697534 | A | AAAATATA others(3): Show |
2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.542+603_542+604ins others(10): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697534 | A | AT | 4 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0003t0010g0225 others(1): Show |
4 | HG00741.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.542+603_542+604ins others(1): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697534 | A | T | 10 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0033g0062 others(7): Show |
13 | HG00621.hp2 HG01175.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+604T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697534 | AAT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
184 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.542+602_542+603del others(2): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697534 | |||||||
| chr12:48697536 | T | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0145 others(29): Show |
44 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.542+602A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697536 | |||||||
| chr12:48697538 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
190 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.542+600A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697538 | |||||||
| chr12:48697540 | T | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0184 others(9): Show |
20 | HG01175.hp2 HG02056.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+598A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697540 | |||||||
| chr12:48697542 | T | A | 4 | a0001c0001t0001g0192 a0001c0002t0003g0016 a0001c0002t0003g0101 others(1): Show |
7 | HG02451.hp1 HG02970.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+596A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697542 | |||||||
| chr12:48697680 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
4 | HG02451.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.542+458C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697680 | |||||||
| chr12:48697717 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.542+421C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697717 | |||||||
| chr12:48697752 | G | A | 1 | a0001c0002t0002g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.542+386C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697752 | |||||||
| chr12:48697839 | T | A | 4 | a0001c0002t0002g0017 a0001c0002t0002g0046 a0001c0002t0002g0112 others(1): Show |
7 | HG00621.hp2 NA18942.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.542+299A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697839 | |||||||
| chr12:48697839 | T | TA | 27 | a0001c0002t0002g0002 a0001c0002t0002g0043 a0001c0002t0002g0045 others(24): Show |
42 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.542+298dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697839 | |||||||
| chr12:48697839 | TA | T | 8 | a0001c0001t0008g0075 a0001c0001t0008g0077 a0001c0001t0021g0055 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.542+298delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697839 | |||||||
| chr12:48697839 | TAA | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0203 others(3): Show |
6 | HG02083.hp1 HG02155.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+297_542+298del others(2): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697839 | |||||||
| chr12:48697847 | AAAAAAAA others(5): Show |
A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.542+279_542+290del others(12): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697847 | |||||||
| chr12:48697851 | A | T | 1 | a0006c0007t0008g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.542+287T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697851 | |||||||
| chr12:48697852 | AAAAAT | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(10): Show |
25 | HG01256.hp1 HG01496.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.542+281_542+285del others(5): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697852 | |||||||
| chr12:48697853 | A | AT | 6 | a0001c0002t0002g0061 a0001c0002t0002g0064 a0001c0002t0002g0065 others(3): Show |
7 | HG01993.hp2 HG02056.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.542+284_542+285ins others(1): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697853 | |||||||
| chr12:48697853 | A | T | 2 | a0001c0001t0008g0077 a0006c0007t0008g0074 |
2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.542+285T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697853 | |||||||
| chr12:48697853 | AAAAT | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
180 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.542+281_542+284del others(4): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697853 | |||||||
| chr12:48697855 | A | AT | 14 | a0001c0002t0002g0007 a0001c0002t0002g0017 a0001c0002t0002g0020 others(11): Show |
18 | HG00621.hp2 HG00738.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.542+282_542+283ins others(1): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697855 | |||||||
| chr12:48697855 | A | ATAT | 3 | a0001c0002t0002g0007 a0001c0002t0002g0020 a0001c0002t0002g0127 |
6 | HG01361.hp1 HG01952.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+282_542+283ins others(3): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697855 | |||||||
| chr12:48697855 | A | T | 32 | a0001c0001t0008g0076 a0001c0001t0008g0077 a0001c0001t0008g0095 others(29): Show |
44 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.542+283T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697855 | |||||||
| chr12:48697855 | AATAT | A | 5 | a0001c0003t0003g0009 a0001c0003t0003g0214 a0001c0003t0003g0218 others(2): Show |
6 | HG01257.hp2 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+279_542+282del others(4): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697855 | |||||||
| chr12:48697857 | T | A | 11 | a0001c0001t0008g0030 a0001c0002t0002g0002 a0001c0002t0002g0003 others(8): Show |
16 | HG01167.hp1 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.542+281A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697857 | |||||||
| chr12:48697857 | T | G | 6 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0203 others(3): Show |
6 | HG02083.hp1 HG02155.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+281A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697857 | |||||||
| chr12:48697859 | T | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(92): Show |
191 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.542+279A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697859 | |||||||
| chr12:48697861 | T | A | 1 | a0001c0003t0003g0220 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.542+277A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697861 | |||||||
| chr12:48697877 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0139 others(16): Show |
32 | HG01346.hp2 HG02015.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.542+261A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48697877 | |||||||
| chr12:48698020 | C | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.542+118G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 6/8 | chr12 | 48698020 | |||||||
| chr12:48698189 | G | GA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(219): Show |
382 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(379): Show |
splice_region_variant&intron_variant | LOW | c.497-7dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698189 | |||||||
| chr12:48698294 | T | C | 6 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(3): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.497-111A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698294 | |||||||
| chr12:48698312 | A | G | 1 | a0001c0002t0002g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497-129T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698312 | |||||||
| chr12:48698548 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.497-365C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698548 | |||||||
| chr12:48698619 | A | G | 14 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(11): Show |
15 | HG02055.hp1 HG02056.hp1 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-436T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698619 | |||||||
| chr12:48698696 | G | A | 20 | a0001c0002t0002g0085 a0001c0003t0003g0009 a0001c0003t0003g0039 others(17): Show |
29 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-513C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698696 | |||||||
| chr12:48698732 | C | T | 3 | a0001c0003t0003g0215 a0001c0003t0003g0216 a0001c0003t0003g0217 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.497-549G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698732 | |||||||
| chr12:48698824 | CGCATGCC others(28): Show |
C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
18 | HG02155.hp2 NA18939.hp1 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-676_497-642del others(35): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698824 | |||||||
| chr12:48698825 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.497-642C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698825 | |||||||
| chr12:48698951 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0134 a0001c0001t0001g0172 others(12): Show |
27 | HG00673.hp2 HG00733.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.497-768G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698951 | |||||||
| chr12:48698956 | CA | C | 12 | a0001c0001t0001g0205 a0001c0002t0002g0114 a0001c0002t0002g0129 others(9): Show |
15 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-774delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48698956 | |||||||
| chr12:48699077 | G | A | 1 | a0001c0003t0003g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.496+701C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699077 | |||||||
| chr12:48699234 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.496+544T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699234 | |||||||
| chr12:48699535 | C | T | 3 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+243G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699535 | |||||||
| chr12:48699544 | C | T | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+234G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699544 | |||||||
| chr12:48699594 | T | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+184A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699594 | |||||||
| chr12:48699625 | A | G | 2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496+153T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699625 | |||||||
| chr12:48699687 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.496+91T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699687 | |||||||
| chr12:48699717 | A | C | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+61T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 5/8 | chr12 | 48699717 | |||||||
| chr12:48699946 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
248 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.434-106G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48699946 | |||||||
| chr12:48700095 | G | A | 1 | a0001c0002t0002g0042 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.434-255C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700095 | |||||||
| chr12:48700184 | T | A | 1 | a0001c0001t0001g0025 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.434-344A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700184 | |||||||
| chr12:48700297 | C | T | 6 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(3): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.434-457G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700297 | |||||||
| chr12:48700318 | C | CA | 7 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(4): Show |
8 | HG02027.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.434-479dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700318 | |||||||
| chr12:48700318 | C | CAA | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0212 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.434-480_434-479dup others(2): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700318 | |||||||
| chr12:48700329 | A | G | 2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.434-489T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700329 | |||||||
| chr12:48700390 | C | CAT | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-552_434-551dup others(2): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700390 | |||||||
| chr12:48700440 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+573C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700440 | |||||||
| chr12:48700681 | C | T | 1 | a0001c0002t0002g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.433+332G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700681 | |||||||
| chr12:48700694 | T | G | 19 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.433+319A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700694 | |||||||
| chr12:48700856 | T | G | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.433+157A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700856 | |||||||
| chr12:48700921 | C | A | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433+92G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700921 | |||||||
| chr12:48700931 | T | G | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433+82A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700931 | |||||||
| chr12:48700982 | A | T | 1 | a0001c0002t0002g0102 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.433+31T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 4/8 | chr12 | 48700982 | |||||||
| chr12:48701146 | C | T | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-73G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701146 | |||||||
| chr12:48701216 | TC | T | 6 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0114 others(3): Show |
6 | HG01515.hp2 HG01517.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-144delG | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701216 | |||||||
| chr12:48701217 | C | CT | 24 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(21): Show |
28 | HG01167.hp1 HG01167.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.373-145dupA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701217 | |||||||
| chr12:48701217 | CTT | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
25 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.373-146_373-145del others(2): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701217 | |||||||
| chr12:48701217 | CTTT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(100): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.373-147_373-145del others(3): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701217 | |||||||
| chr12:48701217 | CTTTT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0037 others(8): Show |
20 | HG02015.hp2 HG02155.hp2 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.373-148_373-145del others(4): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701217 | |||||||
| chr12:48701217 | CTTTTTT | C | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-150_373-145del others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701217 | |||||||
| chr12:48701218 | T | A | 6 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0114 others(3): Show |
6 | HG01515.hp2 HG01517.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-145A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701218 | |||||||
| chr12:48701219 | T | A | 1 | a0001c0002t0002g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.373-146A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701219 | |||||||
| chr12:48701263 | T | TCAC | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
193 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.373-193_373-191dup others(3): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701263 | |||||||
| chr12:48701377 | C | T | 1 | a0001c0002t0023g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.373-304G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701377 | |||||||
| chr12:48701382 | C | A | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0212 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.373-309G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701382 | |||||||
| chr12:48701500 | T | C | 1 | a0001c0002t0002g0127 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.373-427A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701500 | |||||||
| chr12:48701516 | TA | T | 10 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(7): Show |
10 | HG02056.hp1 HG02735.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-444delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701516 | |||||||
| chr12:48701603 | T | C | 36 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0017 others(33): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.373-530A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701603 | |||||||
| chr12:48701638 | G | A | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.373-565C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701638 | |||||||
| chr12:48701641 | C | G | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.373-568G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701641 | |||||||
| chr12:48701873 | T | C | 2 | a0001c0002t0002g0078 a0001c0002t0002g0086 |
2 | HG01256.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.373-800A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701873 | |||||||
| chr12:48701885 | C | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(98): Show |
197 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.373-812G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701885 | |||||||
| chr12:48701899 | C | T | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-826G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701899 | |||||||
| chr12:48701927 | C | T | 3 | a0001c0003t0003g0212 a0001c0003t0003g0214 a0001c0003t0029g0213 |
3 | HG01255.hp1 HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.373-854G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701927 | |||||||
| chr12:48701928 | G | A | 3 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0170 |
3 | HG02015.hp2 HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.373-855C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48701928 | |||||||
| chr12:48702057 | C | T | 4 | a0001c0002t0002g0027 a0001c0002t0002g0042 a0001c0002t0002g0043 others(1): Show |
5 | HG01192.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-984G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702057 | |||||||
| chr12:48702086 | G | A | 1 | a0001c0002t0026g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.373-1013C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702086 | |||||||
| chr12:48702111 | G | A | 5 | a0001c0002t0002g0114 a0001c0002t0002g0129 a0001c0002t0002g0130 others(2): Show |
5 | HG03834.hp1 NA18950.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1038C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702111 | |||||||
| chr12:48702174 | G | C | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-1101C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702174 | |||||||
| chr12:48702357 | T | TAAGAAAA others(342): Show |
1 | a0001c0002t0002g0115 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.373-1285_373-1284i others(351): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702357 | |||||||
| chr12:48702384 | G | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.373-1311C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702384 | |||||||
| chr12:48702458 | C | T | 1 | a0006c0007t0008g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.373-1385G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702458 | |||||||
| chr12:48702492 | A | G | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.373-1419T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702492 | |||||||
| chr12:48702512 | C | T | 2 | a0001c0001t0014g0056 a0001c0001t0014g0057 |
2 | HG01346.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.373-1439G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702512 | |||||||
| chr12:48702513 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.373-1440C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702513 | |||||||
| chr12:48702651 | G | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1578C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702651 | |||||||
| chr12:48702746 | G | C | 1 | a0001c0002t0002g0027 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.373-1673C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702746 | |||||||
| chr12:48702779 | G | A | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.373-1706C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702779 | |||||||
| chr12:48702787 | G | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1714C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702787 | |||||||
| chr12:48702804 | G | A | 7 | a0001c0001t0004g0200 a0001c0001t0009g0036 a0001c0001t0009g0142 others(4): Show |
8 | HG02015.hp2 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-1731C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702804 | |||||||
| chr12:48702835 | T | TGTAGCTA others(6): Show |
1 | a0001c0002t0002g0124 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.373-1775_373-1763d others(15): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702835 | |||||||
| chr12:48702895 | G | A | 1 | a0001c0003t0010g0040 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.373-1822C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702895 | |||||||
| chr12:48702933 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(204): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.373-1860A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702933 | |||||||
| chr12:48702975 | A | G | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1902T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702975 | |||||||
| chr12:48702999 | T | C | 1 | a0001c0002t0002g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.373-1926A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48702999 | |||||||
| chr12:48703137 | G | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-2064C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703137 | |||||||
| chr12:48703140 | T | C | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-2067A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703140 | |||||||
| chr12:48703154 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0198 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.373-2081G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703154 | |||||||
| chr12:48703189 | C | T | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-2116G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703189 | |||||||
| chr12:48703360 | G | A | 2 | a0002c0004t0012g0022 a0005c0008t0012g0136 |
4 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2287C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703360 | |||||||
| chr12:48703429 | C | T | 19 | a0001c0001t0033g0062 a0001c0003t0003g0009 a0001c0003t0003g0039 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.372+2339G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703429 | |||||||
| chr12:48703465 | C | T | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+2303G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703465 | |||||||
| chr12:48703532 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.372+2236G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703532 | |||||||
| chr12:48703556 | A | G | 2 | a0002c0004t0012g0022 a0005c0008t0012g0136 |
4 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2212T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703556 | |||||||
| chr12:48703599 | A | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(175): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.372+2169T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703599 | |||||||
| chr12:48703675 | C | T | 3 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0014g0058 |
3 | HG01346.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.372+2093G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703675 | |||||||
| chr12:48703698 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0208 |
4 | HG03669.hp2 NA18948.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2070C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703698 | |||||||
| chr12:48703710 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.372+2058C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703710 | |||||||
| chr12:48703733 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0190 |
4 | HG02451.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+2035C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703733 | |||||||
| chr12:48703851 | G | A | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.372+1917C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703851 | |||||||
| chr12:48703864 | C | T | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.372+1904G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703864 | |||||||
| chr12:48703867 | G | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+1901C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703867 | |||||||
| chr12:48703907 | C | A | 1 | a0001c0002t0022g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.372+1861G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48703907 | |||||||
| chr12:48704157 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
248 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.372+1611G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704157 | |||||||
| chr12:48704325 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(98): Show |
197 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.372+1443A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704325 | |||||||
| chr12:48704358 | G | C | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.372+1410C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704358 | |||||||
| chr12:48704534 | G | C | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.372+1234C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704534 | |||||||
| chr12:48704620 | C | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+1148G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704620 | |||||||
| chr12:48704723 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(117): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.372+1045G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704723 | |||||||
| chr12:48704754 | A | C | 3 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1014T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704754 | |||||||
| chr12:48704758 | G | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.372+1010C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704758 | |||||||
| chr12:48704846 | C | T | 2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.372+922G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704846 | |||||||
| chr12:48704961 | C | T | 1 | a0001c0003t0003g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.372+807G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48704961 | |||||||
| chr12:48705112 | G | A | 6 | a0001c0001t0001g0198 a0001c0001t0008g0030 a0001c0001t0008g0075 others(3): Show |
7 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+656C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705112 | |||||||
| chr12:48705281 | T | TTTG | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(50): Show |
107 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.372+484_372+486dup others(3): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705281 | |||||||
| chr12:48705281 | T | TTTGTTG | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(43): Show |
86 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.372+481_372+486dup others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705281 | |||||||
| chr12:48705281 | TTTGTTG | T | 3 | a0001c0002t0002g0089 a0001c0002t0002g0090 a0001c0002t0002g0091 |
3 | HG01358.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.372+481_372+486del others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705281 | |||||||
| chr12:48705284 | G | T | 5 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0014g0058 others(2): Show |
5 | HG01346.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+484C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705284 | |||||||
| chr12:48705305 | T | G | 1 | a0001c0002t0002g0116 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.372+463A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705305 | |||||||
| chr12:48705310 | T | C | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.372+458A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705310 | |||||||
| chr12:48705374 | C | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0004g0186 |
3 | HG02129.hp1 NA18957.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.372+394G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705374 | |||||||
| chr12:48705430 | C | CT | 5 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(2): Show |
8 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.372+337dupA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705430 | |||||||
| chr12:48705535 | A | G | 1 | a0001c0003t0003g0215 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.372+233T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705535 | |||||||
| chr12:48705600 | C | T | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+168G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705600 | |||||||
| chr12:48705631 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.372+137G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705631 | |||||||
| chr12:48705708 | T | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0148 others(8): Show |
17 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.372+60A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 3/8 | chr12 | 48705708 | |||||||
| chr12:48706030 | G | A | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.244-134C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706030 | |||||||
| chr12:48706030 | G | GC | 14 | a0001c0001t0001g0018 a0001c0001t0001g0149 a0001c0001t0001g0193 others(11): Show |
17 | HG01993.hp1 HG02027.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.244-135dupG | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706030 | |||||||
| chr12:48706067 | T | C | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-171A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706067 | |||||||
| chr12:48706255 | A | C | 1 | a0001c0001t0021g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244-359T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706255 | |||||||
| chr12:48706287 | G | T | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-391C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706287 | |||||||
| chr12:48706568 | A | G | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG01081.hp2 HG01928.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.244-672T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706568 | |||||||
| chr12:48706573 | A | G | 2 | a0001c0003t0010g0223 a0001c0003t0010g0224 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.244-677T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706573 | |||||||
| chr12:48706594 | C | T | 1 | a0001c0002t0002g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.244-698G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706594 | |||||||
| chr12:48706821 | T | C | 3 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0014g0058 |
3 | HG01346.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.244-925A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706821 | |||||||
| chr12:48706853 | A | T | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-957T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48706853 | |||||||
| chr12:48707052 | C | T | 1 | a0001c0002t0002g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.244-1156G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707052 | |||||||
| chr12:48707127 | C | T | 3 | a0001c0002t0002g0059 a0001c0002t0002g0060 a0001c0002t0002g0061 |
3 | HG02056.hp1 HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.244-1231G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707127 | |||||||
| chr12:48707191 | G | A | 2 | a0001c0001t0004g0200 a0001c0001t0009g0199 |
2 | NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.244-1295C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707191 | |||||||
| chr12:48707259 | G | A | 1 | a0001c0002t0032g0117 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.244-1363C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707259 | |||||||
| chr12:48707280 | TTTTC | T | 5 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0018g0097 others(2): Show |
8 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-1388_244-1385d others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707280 | |||||||
| chr12:48707288 | CT | C | 12 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(9): Show |
12 | HG00323.hp1 HG03491.hp2 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.244-1393delA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707288 | |||||||
| chr12:48707292 | T | C | 1 | a0001c0002t0002g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.244-1396A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707292 | |||||||
| chr12:48707406 | C | T | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244-1510G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707406 | |||||||
| chr12:48707622 | C | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-1726G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707622 | |||||||
| chr12:48707623 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
9 | HG00423.hp1 HG00558.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.244-1727C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707623 | |||||||
| chr12:48707662 | G | GTTA | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1767_244-1766i others(5): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707662 | |||||||
| chr12:48707665 | C | T | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1769G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707665 | |||||||
| chr12:48707666 | C | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1770G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707666 | |||||||
| chr12:48707670 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1774C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707670 | |||||||
| chr12:48707673 | A | ATTATTAT others(45): Show |
5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1778_244-1777i others(54): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707673 | |||||||
| chr12:48707743 | G | A | 1 | a0001c0002t0002g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.244-1847C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707743 | |||||||
| chr12:48707887 | G | A | 1 | a0001c0002t0002g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.244-1991C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707887 | |||||||
| chr12:48707963 | C | G | 14 | a0001c0001t0001g0031 a0001c0003t0003g0009 a0001c0003t0003g0039 others(11): Show |
23 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.244-2067G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48707963 | |||||||
| chr12:48708059 | C | T | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.244-2163G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708059 | |||||||
| chr12:48708184 | C | T | 3 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-2288G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708184 | |||||||
| chr12:48708186 | T | C | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-2290A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708186 | |||||||
| chr12:48708362 | C | T | 1 | a0001c0001t0033g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244-2466G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708362 | |||||||
| chr12:48708373 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
248 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.244-2477A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708373 | |||||||
| chr12:48708391 | A | G | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.244-2495T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708391 | |||||||
| chr12:48708427 | G | A | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.244-2531C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708427 | |||||||
| chr12:48708504 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(117): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.244-2608C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708504 | |||||||
| chr12:48708538 | C | T | 1 | a0001c0001t0004g0152 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.244-2642G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708538 | |||||||
| chr12:48708557 | A | G | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.244-2661T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708557 | |||||||
| chr12:48708850 | T | C | 1 | a0001c0002t0002g0043 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244-2954A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48708850 | |||||||
| chr12:48709153 | A | G | 3 | a0001c0001t0001g0151 a0002c0004t0012g0022 a0005c0008t0012g0136 |
5 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-3257T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709153 | |||||||
| chr12:48709461 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-3565C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709461 | |||||||
| chr12:48709549 | A | C | 1 | a0001c0002t0002g0104 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.244-3653T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709549 | |||||||
| chr12:48709587 | T | C | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.244-3691A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709587 | |||||||
| chr12:48709649 | A | G | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-3753T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709649 | |||||||
| chr12:48709732 | C | T | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-3836G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709732 | |||||||
| chr12:48709895 | A | ATTTT | 3 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-4003_244-4000d others(6): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48709895 | |||||||
| chr12:48710041 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18988.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.244-4145C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710041 | |||||||
| chr12:48710052 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.244-4156G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710052 | |||||||
| chr12:48710184 | GC | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
193 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.243+4258delG | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710184 | |||||||
| chr12:48710403 | T | C | 2 | a0001c0002t0002g0064 a0001c0002t0002g0065 |
2 | NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.243+4040A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710403 | |||||||
| chr12:48710545 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
248 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.243+3898T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710545 | |||||||
| chr12:48710603 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.243+3840C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710603 | |||||||
| chr12:48710612 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.243+3831G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710612 | |||||||
| chr12:48710677 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.243+3766C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710677 | |||||||
| chr12:48710934 | G | C | 5 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0014g0058 others(2): Show |
5 | HG01346.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3509C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710934 | |||||||
| chr12:48710954 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243+3489C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710954 | |||||||
| chr12:48710955 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
193 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.243+3488C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48710955 | |||||||
| chr12:48711124 | G | A | 2 | a0001c0002t0003g0016 a0001c0002t0003g0101 |
5 | HG02451.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3319C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711124 | |||||||
| chr12:48711152 | C | T | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+3291G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711152 | |||||||
| chr12:48711249 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
18 | HG02155.hp2 NA18939.hp1 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+3194C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711249 | |||||||
| chr12:48711476 | G | A | 19 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.243+2967C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711476 | |||||||
| chr12:48711492 | T | C | 1 | a0001c0002t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.243+2951A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711492 | |||||||
| chr12:48711521 | C | T | 19 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.243+2922G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711521 | |||||||
| chr12:48711661 | C | T | 1 | a0001c0003t0003g0039 | 2 | HG00323.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.243+2782G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711661 | |||||||
| chr12:48711705 | CAG | C | 3 | a0001c0001t0007g0004 a0001c0001t0007g0146 a0001c0001t0007g0147 |
12 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.243+2736_243+2737d others(4): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711705 | |||||||
| chr12:48711736 | A | G | 3 | a0001c0003t0003g0212 a0001c0003t0003g0214 a0001c0003t0029g0213 |
3 | HG01255.hp1 HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.243+2707T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711736 | |||||||
| chr12:48711749 | C | T | 1 | a0001c0002t0016g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.243+2694G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711749 | |||||||
| chr12:48711938 | G | A | 4 | a0001c0002t0002g0021 a0001c0002t0002g0119 a0001c0002t0002g0120 others(1): Show |
6 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+2505C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711938 | |||||||
| chr12:48711950 | G | A | 7 | a0001c0001t0001g0208 a0001c0002t0003g0016 a0001c0002t0003g0099 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+2493C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711950 | |||||||
| chr12:48711953 | C | T | 1 | a0001c0002t0002g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.243+2490G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48711953 | |||||||
| chr12:48712026 | C | T | 19 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.243+2417G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712026 | |||||||
| chr12:48712055 | A | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.243+2388T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712055 | |||||||
| chr12:48712280 | A | G | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+2163T>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712280 | |||||||
| chr12:48712340 | T | C | 1 | a0001c0002t0022g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.243+2103A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712340 | |||||||
| chr12:48712362 | C | G | 1 | a0001c0001t0008g0030 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.243+2081G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712362 | |||||||
| chr12:48712423 | GA | G | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+2019delT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712423 | |||||||
| chr12:48712432 | C | T | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.243+2011G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712432 | |||||||
| chr12:48712578 | TTAAAAAA others(9): Show |
T | 32 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0017 others(29): Show |
61 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.243+1849_243+1864d others(18): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712578 | |||||||
| chr12:48712579 | T | TA | 8 | a0001c0001t0033g0062 a0001c0002t0002g0003 a0001c0002t0002g0048 others(5): Show |
13 | HG00639.hp2 HG00738.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.243+1863dupT | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712579 | |||||||
| chr12:48712579 | TAAAAAAA others(10): Show |
T | 5 | a0001c0002t0002g0123 a0001c0002t0002g0124 a0001c0002t0002g0128 others(2): Show |
5 | HG00738.hp2 NA18747.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+1847_243+1863d others(19): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712579 | |||||||
| chr12:48712579 | TAAAAAAA others(12): Show |
T | 3 | a0001c0001t0014g0056 a0001c0001t0014g0057 a0001c0001t0014g0058 |
3 | HG01346.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.243+1845_243+1863d others(21): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712579 | |||||||
| chr12:48712579 | TAAAAAAA others(14): Show |
T | 1 | a0001c0003t0003g0212 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.243+1843_243+1863d others(23): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712579 | |||||||
| chr12:48712579 | TAAAAAAA others(18): Show |
T | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+1839_243+1863d others(27): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712579 | |||||||
| chr12:48712580 | A | T | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.243+1863T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712580 | |||||||
| chr12:48712580 | AAAAAAAA others(8): Show |
A | 6 | a0001c0002t0002g0028 a0001c0002t0002g0049 a0001c0002t0002g0051 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+1848_243+1862d others(17): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712580 | |||||||
| chr12:48712581 | AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0027g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.243+1848_243+1861d others(16): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712581 | |||||||
| chr12:48712582 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0004g0006 a0001c0002t0002g0028 |
2 | NA18747.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.243+1848_243+1860d others(15): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712582 | |||||||
| chr12:48712583 | AAAAAAAA others(5): Show |
A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(4): Show |
7 | HG01256.hp1 HG02004.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1848_243+1859d others(14): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712583 | |||||||
| chr12:48712584 | AAAAAAAA others(4): Show |
A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(82): Show |
165 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.243+1848_243+1858d others(13): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712584 | |||||||
| chr12:48712585 | AAAAAAAA others(3): Show |
A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(34): Show |
47 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.243+1848_243+1857d others(12): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712585 | |||||||
| chr12:48712590 | AAAAAT | A | 6 | a0001c0001t0008g0095 a0001c0001t0008g0096 a0001c0002t0002g0071 others(3): Show |
6 | HG01167.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+1848_243+1852d others(7): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712590 | |||||||
| chr12:48712593 | AAT | A | 9 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(6): Show |
10 | HG01192.hp1 HG02818.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+1848_243+1849d others(4): Show |
CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712593 | |||||||
| chr12:48712594 | AT | A | 12 | a0001c0002t0002g0010 a0001c0002t0002g0045 a0001c0002t0002g0046 others(9): Show |
18 | HG01071.hp2 HG01099.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.243+1848delA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712594 | |||||||
| chr12:48712595 | T | A | 20 | a0001c0001t0033g0062 a0001c0002t0002g0003 a0001c0002t0002g0027 others(17): Show |
32 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.243+1848A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712595 | |||||||
| chr12:48712601 | A | T | 2 | a0001c0002t0002g0066 a0001c0003t0003g0212 |
2 | HG03471.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.243+1842T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712601 | |||||||
| chr12:48712615 | A | T | 3 | a0001c0002t0002g0066 a0003c0006t0002g0067 a0003c0006t0025g0068 |
3 | HG01167.hp2 HG01169.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.243+1828T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712615 | |||||||
| chr12:48712637 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.243+1806G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712637 | |||||||
| chr12:48712644 | C | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0004c0005t0001g0140 others(1): Show |
4 | NA18941.hp2 NA18983.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1799G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712644 | |||||||
| chr12:48712649 | T | C | 7 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(4): Show |
7 | NA18942.hp1 NA18979.hp2 NA19057.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+1794A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712649 | |||||||
| chr12:48712724 | G | C | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+1719C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712724 | |||||||
| chr12:48712756 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0075 a0001c0001t0008g0076 others(2): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+1687C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712756 | |||||||
| chr12:48712956 | A | C | 3 | a0001c0001t0007g0004 a0001c0001t0007g0146 a0001c0001t0007g0147 |
12 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.243+1487T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48712956 | |||||||
| chr12:48713177 | G | A | 8 | a0001c0002t0002g0066 a0001c0002t0002g0069 a0001c0002t0002g0070 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+1266C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713177 | |||||||
| chr12:48713190 | T | A | 1 | a0001c0002t0022g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.243+1253A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713190 | |||||||
| chr12:48713200 | C | CT | 10 | a0001c0002t0002g0027 a0001c0002t0002g0042 a0001c0002t0002g0043 others(7): Show |
11 | HG01192.hp1 HG01978.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.243+1242dupA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713200 | |||||||
| chr12:48713200 | CT | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
234 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.243+1242delA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713200 | |||||||
| chr12:48713224 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
193 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.243+1219C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713224 | |||||||
| chr12:48713235 | G | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+1208C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713235 | |||||||
| chr12:48713515 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(98): Show |
197 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.243+928C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713515 | |||||||
| chr12:48713560 | G | A | 2 | a0002c0004t0012g0022 a0005c0008t0012g0136 |
4 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+883C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713560 | |||||||
| chr12:48713632 | T | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+811A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713632 | |||||||
| chr12:48713719 | G | C | 19 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0137 others(16): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.243+724C>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713719 | |||||||
| chr12:48713770 | C | A | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.243+673G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713770 | |||||||
| chr12:48713898 | T | A | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.243+545A>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713898 | |||||||
| chr12:48713903 | G | GT | 4 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+539dupA | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713903 | |||||||
| chr12:48713919 | G | A | 1 | a0001c0001t0001g0038 | 2 | NA19058.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.243+524C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713919 | |||||||
| chr12:48713973 | C | A | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0212 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.243+470G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 2/8 | chr12 | 48713973 | |||||||
| chr12:48714705 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(204): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.162-181G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48714705 | |||||||
| chr12:48714880 | T | G | 1 | a0001c0003t0003g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162-356A>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48714880 | |||||||
| chr12:48714916 | G | A | 2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.162-392C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48714916 | |||||||
| chr12:48715170 | A | C | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162-646T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715170 | |||||||
| chr12:48715173 | G | A | 2 | a0001c0002t0002g0126 a0001c0002t0002g0127 |
2 | NA18993.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.162-649C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715173 | |||||||
| chr12:48715186 | A | C | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162-662T>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715186 | |||||||
| chr12:48715254 | C | A | 1 | a0001c0003t0010g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162-730G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715254 | |||||||
| chr12:48715254 | C | T | 1 | a0004c0005t0001g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.162-730G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715254 | |||||||
| chr12:48715315 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.162-791G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715315 | |||||||
| chr12:48715453 | A | T | 2 | a0001c0002t0018g0097 a0001c0002t0018g0098 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162-929T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715453 | |||||||
| chr12:48715661 | T | C | 1 | a0001c0002t0002g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161+854A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715661 | |||||||
| chr12:48715799 | C | G | 1 | a0001c0001t0013g0138 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.161+716G>C | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715799 | |||||||
| chr12:48715806 | T | C | 4 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 others(1): Show |
4 | HG03834.hp1 NA18950.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+709A>G | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715806 | |||||||
| chr12:48715820 | G | A | 7 | a0001c0002t0003g0016 a0001c0002t0003g0099 a0001c0002t0003g0101 others(4): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+695C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715820 | |||||||
| chr12:48715855 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
193 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.161+660C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715855 | |||||||
| chr12:48715881 | C | T | 1 | a0001c0002t0011g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+634G>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715881 | |||||||
| chr12:48715968 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.161+547T>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48715968 | |||||||
| chr12:48716040 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.161+475C>A | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716040 | |||||||
| chr12:48716248 | G | A | 36 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0017 others(33): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+267C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716248 | |||||||
| chr12:48716324 | G | A | 1 | a0001c0009t0003g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.161+191C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716324 | |||||||
| chr12:48716440 | C | A | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0212 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+75G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716440 | |||||||
| chr12:48716442 | C | A | 18 | a0001c0003t0003g0009 a0001c0003t0003g0039 a0001c0003t0003g0212 others(15): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+73G>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716442 | |||||||
| chr12:48716465 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(117): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.161+50C>T | CCNT1 | ENSG00000129315.12 | transcript | ENST00000261900.8 | protein_coding | 1/8 | chr12 | 48716465 |