Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10576 |
| ensemblid | ENSG00000166226.13 |
| hgncid | 1615 |
| symbol | CCT2 |
| name | chaperonin containing TCP1 subunit 2 |
| refseq_nuc | NM_006431.3 |
| refseq_prot | NP_006422.1 |
| ensembl_nuc | ENST00000299300.11 |
| ensembl_prot | ENSP00000299300.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 69585459 |
| end | 69601570 |
| strand | + |
| ver | v1.2 |
| region | chr12:69585459-69601570 |
| region5000 | chr12:69580459-69606570 |
| regionname0 | CCT2_chr12_69585459_69601570 |
| regionname5000 | CCT2_chr12_69580459_69606570 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 535 | 407 | 98 | 69 | 194 | 14 | 30 | 154 | CCT2_chr12_69580459_69606570 | CCT2 | MASLS others(530): Show |
chr12 | 69580459 | 69606570 |
| a0002 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | MASLS others(530): Show |
chr12 | 69580459 | 69606570 |
| a0003 | 0/0 | 535 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | MASLS others(530): Show |
chr12 | 69580459 | 69606570 |
| a0004 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | MASLS others(530): Show |
chr12 | 69580459 | 69606570 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1605 | 319 | 88 | 50 | 148 | 10 | 21 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0001c0002 | 0/0 | 1605 | 86 | 10 | 19 | 45 | 4 | 8 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0001c0003 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0001c0006 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0002c0007 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0003c0004 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 | ||
| a0004c0005 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | ATGGC others(1600): Show |
chr12 | 69580459 | 69606570 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1916 | 300 | 72 | 48 | 148 | 10 | 20 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0001t0003 | 0/0 | 1916 | 17 | 15 | 2 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0001t0005 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0001t0006 | 0/0 | 1916 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0002t0001 | 0/0 | 1916 | 9 | 0 | 0 | 7 | 1 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0002t0002 | 0/0 | 1916 | 76 | 9 | 19 | 38 | 3 | 7 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0002t0004 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0003t0001 | 0/0 | 1916 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0001c0006t0001 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0002c0007t0001 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0003c0004t0001 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| a0004c0005t0001 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | AGTCC others(1911): Show |
chr12 | 69580459 | 69606570 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 51 | 0 | 3 | 47 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0002 | 0/0 | 51 | 5 | 7 | 30 | 2 | 7 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0004 | 1/1 | 20 | 1 | 5 | 7 | 5 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0005 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0008 | 0/0 | 8 | 1 | 7 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0013 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0016 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0003 | 0/0 | 36 | 3 | 10 | 15 | 3 | 5 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0006 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0002c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0003c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| a0004c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | GBR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00597 | hp2 | a0002 | c0007 | t0001 | g0002 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00621 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | CHS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01981 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02083 | hp1 | a0004 | c0005 | t0001 | g0004 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | BEB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | STU | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ASW | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | TSI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | GIH | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | LWK | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CCT2_chr12_69580459_69606570 | CCT2 | chr12 | 69580459 | 69606570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69592106 | G | C | 1 | a0003 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.697G>C | p.Glu233Gln | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/16 | 760/1916 | 697/1608 | 233/535 | chr12 | 69592106 | |||
| chr12:69597664 | G | T | 1 | a0002 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1129G>T | p.Gly377Cys | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/16 | 1192/1916 | 1129/1608 | 377/535 | chr12 | 69597664 | |||
| chr12:69599904 | A | G | 1 | a0004 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1477A>G | p.Ile493Val | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/16 | 1540/1916 | 1477/1608 | 493/535 | chr12 | 69599904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69586302 | T | C | 1 | a0001c0003 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.36T>C | p.Phe12Phe | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/16 | 99/1916 | 36/1608 | 12/535 | chr12 | 69586302 | |||
| chr12:69593008 | A | G | 1 | a0001c0002 | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
synonymous_variant | LOW | c.783A>G | p.Thr261Thr | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 9/16 | 846/1916 | 783/1608 | 261/535 | chr12 | 69593008 | |||
| chr12:69597678 | A | G | 1 | a0001c0006 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.1143A>G | p.Gln381Gln | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/16 | 1206/1916 | 1143/1608 | 381/535 | chr12 | 69597678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69601390 | A | G | 1 | a0001c0001t0006 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 65 | chr12 | 69601390 | ||||||
| chr12:69601461 | C | T | 1 | a0001c0001t0005 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*136C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 136 | chr12 | 69601461 | ||||||
| chr12:69601490 | G | A | 1 | a0001c0002t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 165 | chr12 | 69601490 | ||||||
| chr12:69601493 | T | C | 1 | a0001c0002t0002 | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*168T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 168 | chr12 | 69601493 | ||||||
| chr12:69601546 | A | G | 1 | a0001c0001t0003 | 17 | HG01109.hp2 HG01361.hp2 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*221A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 221 | chr12 | 69601546 | ||||||
| chr12:69601567 | A | G | 1 | a0001c0002t0002 | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*242A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 16/16 | 242 | chr12 | 69601567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69585552 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3+28C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585552 | |||||||
| chr12:69585685 | C | G | 1 | a0001c0002t0002g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3+161C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585685 | |||||||
| chr12:69585737 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
134 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.3+213C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585737 | |||||||
| chr12:69585740 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0042 |
9 | HG01167.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+216C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585740 | |||||||
| chr12:69585745 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3+221G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585745 | |||||||
| chr12:69585791 | C | T | 1 | a0001c0002t0002g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3+267C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69585791 | |||||||
| chr12:69586051 | CG | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-214delG | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 69586051 | ||||||
| chr12:69586215 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4-55G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69586215 | |||||||
| chr12:69586236 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4-34C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69586236 | |||||||
| chr12:69586248 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
333 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.4-22G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 1/15 | chr12 | 69586248 | |||||||
| chr12:69586361 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
367 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(364): Show |
intron_variant | MODIFIER | c.78+17G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586361 | |||||||
| chr12:69586433 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.78+89C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586433 | |||||||
| chr12:69586529 | G | A | 1 | a0001c0002t0002g0033 | 2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.78+185G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586529 | |||||||
| chr12:69586550 | C | G | 1 | a0001c0002t0002g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.79-203C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586550 | |||||||
| chr12:69586603 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79-150G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586603 | |||||||
| chr12:69586654 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(15): Show |
88 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.79-99C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586654 | |||||||
| chr12:69586698 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.79-55C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 2/15 | chr12 | 69586698 | |||||||
| chr12:69586836 | GTTTTATA others(12): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.144+22_144+40delTA others(17): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 69586836 | ||||||
| chr12:69586865 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144+47C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69586865 | |||||||
| chr12:69587013 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.144+195C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587013 | |||||||
| chr12:69587028 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.144+210C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587028 | |||||||
| chr12:69587114 | CAG | C | 1 | a0001c0001t0003g0011 | 6 | HG02055.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.144+298_144+299del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 69587114 | ||||||
| chr12:69587250 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-255G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587250 | |||||||
| chr12:69587306 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.145-199A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587306 | |||||||
| chr12:69587331 | G | A | 23 | a0001c0002t0001g0010 a0001c0002t0001g0054 a0001c0002t0001g0064 others(20): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.145-174G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587331 | |||||||
| chr12:69587347 | GTT | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0042 |
6 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-157_145-156del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587347 | |||||||
| chr12:69587363 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.145-142A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 3/15 | chr12 | 69587363 | |||||||
| chr12:69587706 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0124 |
4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.256+90C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 4/15 | chr12 | 69587706 | |||||||
| chr12:69587892 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.257-38G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 4/15 | chr12 | 69587892 | |||||||
| chr12:69588082 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(98): Show |
334 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.334-68G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 5/15 | chr12 | 69588082 | |||||||
| chr12:69588349 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
240 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.446+87G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588349 | |||||||
| chr12:69588355 | A | C | 8 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0035 others(5): Show |
16 | HG01109.hp2 HG01361.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+93A>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588355 | |||||||
| chr12:69588438 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.446+176G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588438 | |||||||
| chr12:69588483 | C | T | 4 | a0001c0001t0003g0026 a0001c0001t0003g0079 a0001c0001t0003g0080 others(1): Show |
6 | HG01109.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+221C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588483 | |||||||
| chr12:69588491 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.446+229A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588491 | |||||||
| chr12:69588517 | C | T | 9 | a0001c0001t0001g0023 a0001c0001t0003g0011 a0001c0001t0003g0026 others(6): Show |
19 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.446+255C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588517 | |||||||
| chr12:69588601 | T | A | 1 | a0001c0002t0002g0047 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.446+339T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588601 | |||||||
| chr12:69588627 | C | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0082 |
3 | HG01361.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.446+365C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588627 | |||||||
| chr12:69588904 | T | TA | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.447-580dupA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 69588904 | ||||||
| chr12:69588968 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.447-517G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588968 | |||||||
| chr12:69588997 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.447-488C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69588997 | |||||||
| chr12:69589074 | A | G | 25 | a0001c0002t0001g0010 a0001c0002t0001g0036 a0001c0002t0001g0054 others(22): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.447-411A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589074 | |||||||
| chr12:69589221 | G | A | 4 | a0001c0001t0003g0026 a0001c0001t0003g0079 a0001c0001t0003g0080 others(1): Show |
6 | HG01109.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.447-264G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589221 | |||||||
| chr12:69589248 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.447-237T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589248 | |||||||
| chr12:69589268 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.447-217T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589268 | |||||||
| chr12:69589282 | CT | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0003g0084 others(1): Show |
7 | HG01167.hp1 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.447-193delT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 69589282 | ||||||
| chr12:69589282 | CTT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
279 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(276): Show |
intron_variant | MODIFIER | c.447-194_447-193del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 69589282 | ||||||
| chr12:69589291 | T | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.447-194T>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589291 | |||||||
| chr12:69589324 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.447-161A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 6/15 | chr12 | 69589324 | |||||||
| chr12:69589735 | C | A | 9 | a0001c0001t0001g0023 a0001c0001t0003g0011 a0001c0001t0003g0026 others(6): Show |
19 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.649+48C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69589735 | |||||||
| chr12:69589845 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.649+158T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69589845 | |||||||
| chr12:69589861 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.649+174C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69589861 | |||||||
| chr12:69589949 | T | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0124 |
4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+262T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69589949 | |||||||
| chr12:69590004 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0042 others(7): Show |
24 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.649+317T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590004 | |||||||
| chr12:69590213 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.649+526A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590213 | |||||||
| chr12:69590226 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
236 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.649+539G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590226 | |||||||
| chr12:69590294 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.649+607G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590294 | |||||||
| chr12:69590302 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.649+615A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590302 | |||||||
| chr12:69590682 | CTTGA | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(20): Show |
98 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.649+998_649+1001de others(5): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69590682 | ||||||
| chr12:69590719 | C | CT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG01361.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.649+1047dupT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69590719 | ||||||
| chr12:69590719 | C | CTT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
221 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.649+1046_649+1047d others(4): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69590719 | ||||||
| chr12:69590719 | C | CTTT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0076 |
9 | HG01099.hp2 HG01192.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.649+1045_649+1047d others(5): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69590719 | ||||||
| chr12:69590719 | CT | C | 22 | a0001c0001t0003g0079 a0001c0002t0001g0010 a0001c0002t0001g0054 others(19): Show |
83 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.649+1047delT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69590719 | ||||||
| chr12:69590739 | C | T | 1 | a0001c0001t0001g0013 | 6 | HG00639.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.649+1052C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590739 | |||||||
| chr12:69590803 | G | C | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.649+1116G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590803 | |||||||
| chr12:69590891 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.650-1168G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590891 | |||||||
| chr12:69590926 | CCAGGCTG | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0083 others(1): Show |
7 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.650-1132_650-1126d others(9): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590926 | |||||||
| chr12:69590960 | C | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(20): Show |
98 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.650-1099C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590960 | |||||||
| chr12:69590984 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0042 others(7): Show |
24 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.650-1075A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69590984 | |||||||
| chr12:69591003 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.650-1056G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591003 | |||||||
| chr12:69591023 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.650-1036C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591023 | |||||||
| chr12:69591238 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.650-821C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591238 | |||||||
| chr12:69591388 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
283 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(280): Show |
intron_variant | MODIFIER | c.650-671G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591388 | |||||||
| chr12:69591396 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02970.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.650-663T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591396 | |||||||
| chr12:69591408 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.650-651C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591408 | |||||||
| chr12:69591525 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0122 |
2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.650-534C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591525 | |||||||
| chr12:69591535 | TATA | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
283 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(280): Show |
intron_variant | MODIFIER | c.650-523_650-521del others(3): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591535 | |||||||
| chr12:69591537 | T | A | 1 | a0001c0001t0001g0004 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650-522T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591537 | |||||||
| chr12:69591590 | G | A | 2 | a0001c0002t0002g0015 a0001c0002t0002g0056 |
6 | HG00673.hp2 NA18960.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-469G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591590 | |||||||
| chr12:69591672 | T | A | 25 | a0001c0002t0001g0010 a0001c0002t0001g0036 a0001c0002t0001g0054 others(22): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.650-387T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591672 | |||||||
| chr12:69591696 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
138 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.650-363G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591696 | |||||||
| chr12:69591756 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
138 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.650-303A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591756 | |||||||
| chr12:69591841 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.650-218A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591841 | |||||||
| chr12:69591879 | AAAC | A | 23 | a0001c0002t0001g0010 a0001c0002t0001g0054 a0001c0002t0001g0064 others(20): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.650-172_650-170del others(3): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69591879 | ||||||
| chr12:69591891 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.650-168A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | chr12 | 69591891 | |||||||
| chr12:69591991 | CTT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
269 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.650-64_650-63delTT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 69591991 | ||||||
| chr12:69592253 | A | T | 1 | a0001c0002t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.750+94A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592253 | |||||||
| chr12:69592313 | T | TA | 4 | a0001c0002t0002g0009 a0001c0002t0002g0047 a0001c0002t0002g0048 others(1): Show |
9 | HG00544.hp2 NA18955.hp2 NA18992.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+167dupA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 69592313 | ||||||
| chr12:69592313 | TA | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.750+167delA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 69592313 | ||||||
| chr12:69592375 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0023 others(12): Show |
33 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.750+216C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592375 | |||||||
| chr12:69592393 | G | T | 1 | a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.750+234G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592393 | |||||||
| chr12:69592409 | G | C | 1 | a0001c0003t0001g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.750+250G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592409 | |||||||
| chr12:69592415 | G | A | 1 | a0001c0002t0002g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.750+256G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592415 | |||||||
| chr12:69592431 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0083 others(2): Show |
8 | HG01884.hp1 HG02004.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.750+272C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592431 | |||||||
| chr12:69592492 | CA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(107): Show |
357 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.750+346delA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 69592492 | ||||||
| chr12:69592558 | G | T | 1 | a0001c0002t0002g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.750+399G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592558 | |||||||
| chr12:69592568 | A | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0023 others(12): Show |
33 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.751-408A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592568 | |||||||
| chr12:69592577 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0097 a0001c0001t0001g0100 others(2): Show |
10 | HG00741.hp2 HG01069.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.751-399A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592577 | |||||||
| chr12:69592592 | C | T | 1 | a0001c0001t0001g0030 | 3 | HG01099.hp1 HG02273.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.751-384C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592592 | |||||||
| chr12:69592626 | CTT | C | 15 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0023 others(12): Show |
33 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.751-348_751-347del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 69592626 | ||||||
| chr12:69592627 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.751-349T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592627 | |||||||
| chr12:69592647 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.751-329C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592647 | |||||||
| chr12:69592708 | A | G | 1 | a0001c0001t0001g0029 | 3 | NA18970.hp2 NA19003.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.751-268A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592708 | |||||||
| chr12:69592716 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.751-260A>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592716 | |||||||
| chr12:69592794 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.751-182G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592794 | |||||||
| chr12:69592887 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.751-89C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592887 | |||||||
| chr12:69592901 | C | T | 1 | a0001c0002t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.751-75C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592901 | |||||||
| chr12:69592964 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.751-12C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592964 | |||||||
| chr12:69592969 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | splice_region_variant&intron_variant | LOW | c.751-7G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 8/15 | chr12 | 69592969 | |||||||
| chr12:69593220 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.878+117A>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 9/15 | chr12 | 69593220 | |||||||
| chr12:69593337 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.879-173T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 9/15 | chr12 | 69593337 | |||||||
| chr12:69593714 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
341 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.982+101G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69593714 | |||||||
| chr12:69593743 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.982+130T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69593743 | |||||||
| chr12:69593796 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982+183C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69593796 | |||||||
| chr12:69593974 | C | CA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(17): Show |
97 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.982+373dupA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69593974 | ||||||
| chr12:69594030 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.982+417G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594030 | |||||||
| chr12:69594030 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.982+417G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594030 | |||||||
| chr12:69594052 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.982+439T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594052 | |||||||
| chr12:69594054 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0117 |
3 | HG02970.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.982+441G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594054 | |||||||
| chr12:69594067 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0059 |
5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+454A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594067 | |||||||
| chr12:69594090 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.982+477G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594090 | |||||||
| chr12:69594103 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.982+490C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594103 | |||||||
| chr12:69594138 | CA | C | 9 | a0001c0001t0001g0023 a0001c0001t0003g0011 a0001c0001t0003g0026 others(6): Show |
19 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.982+538delA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594138 | ||||||
| chr12:69594156 | T | C | 23 | a0001c0002t0001g0036 a0001c0002t0001g0064 a0001c0002t0002g0003 others(20): Show |
79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.982+543T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594156 | |||||||
| chr12:69594188 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
370 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.982+575G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594188 | |||||||
| chr12:69594227 | T | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.982+614T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594227 | |||||||
| chr12:69594311 | A | G | 25 | a0001c0002t0001g0010 a0001c0002t0001g0036 a0001c0002t0001g0054 others(22): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.982+698A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594311 | |||||||
| chr12:69594401 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.982+788T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594401 | |||||||
| chr12:69594406 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.982+793G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594406 | |||||||
| chr12:69594429 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.982+816G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594429 | |||||||
| chr12:69594466 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.982+853C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594466 | |||||||
| chr12:69594690 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982+1077A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594690 | |||||||
| chr12:69594730 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.982+1117C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594730 | |||||||
| chr12:69594803 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.982+1190G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594803 | |||||||
| chr12:69594837 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.982+1224C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594837 | |||||||
| chr12:69594843 | CT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(18): Show |
98 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.982+1233delT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594843 | ||||||
| chr12:69594846 | T | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+1233T>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594846 | |||||||
| chr12:69594846 | T | TA | 9 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0003g0011 others(6): Show |
19 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.982+1250dupA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594846 | ||||||
| chr12:69594846 | TA | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0034 others(16): Show |
42 | HG00544.hp2 HG00673.hp2 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.982+1250delA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594846 | ||||||
| chr12:69594846 | TAA | T | 11 | a0001c0002t0001g0064 a0001c0002t0002g0003 a0001c0002t0002g0024 others(8): Show |
49 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.982+1249_982+1250d others(4): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594846 | ||||||
| chr12:69594846 | TAAA | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
13 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.982+1248_982+1250d others(5): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69594846 | ||||||
| chr12:69594847 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(18): Show |
98 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.982+1234A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594847 | |||||||
| chr12:69594858 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.982+1245A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594858 | |||||||
| chr12:69594944 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.982+1331A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69594944 | |||||||
| chr12:69595033 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0112 |
4 | NA18953.hp1 NA18970.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+1420G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595033 | |||||||
| chr12:69595069 | A | AGGAGACC others(1): Show |
119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
371 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.982+1459_982+1466d others(10): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69595069 | ||||||
| chr12:69595095 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0003g0011 a0001c0001t0003g0026 others(6): Show |
19 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.982+1482G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595095 | |||||||
| chr12:69595206 | G | T | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.982+1593G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595206 | |||||||
| chr12:69595275 | G | A | 8 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0035 others(5): Show |
16 | HG01109.hp2 HG01361.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.982+1662G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595275 | |||||||
| chr12:69595533 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
371 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.983-1623A>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595533 | |||||||
| chr12:69595612 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.983-1544C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595612 | |||||||
| chr12:69595688 | C | CA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(64): Show |
171 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.983-1449dupA | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69595688 | ||||||
| chr12:69595688 | C | CAA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(24): Show |
113 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.983-1450_983-1449d others(4): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69595688 | ||||||
| chr12:69595688 | C | CAAA | 3 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0069 |
6 | HG01934.hp1 HG03041.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-1451_983-1449d others(5): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69595688 | ||||||
| chr12:69595762 | C | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0079 others(2): Show |
12 | HG01109.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.983-1394C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595762 | |||||||
| chr12:69595793 | ATGT | A | 21 | a0001c0002t0001g0064 a0001c0002t0002g0003 a0001c0002t0002g0006 others(18): Show |
77 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.983-1361_983-1359d others(5): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69595793 | ||||||
| chr12:69595950 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(100): Show |
340 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(337): Show |
intron_variant | MODIFIER | c.983-1206C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69595950 | |||||||
| chr12:69596042 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.983-1114C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596042 | |||||||
| chr12:69596119 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
249 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(246): Show |
intron_variant | MODIFIER | c.983-1037T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596119 | |||||||
| chr12:69596178 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.983-978A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596178 | |||||||
| chr12:69596179 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-977C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596179 | |||||||
| chr12:69596243 | TATG | T | 21 | a0001c0002t0001g0064 a0001c0002t0002g0003 a0001c0002t0002g0006 others(18): Show |
77 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.983-911_983-909del others(3): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 69596243 | ||||||
| chr12:69596293 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(22): Show |
105 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.983-863A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596293 | |||||||
| chr12:69596627 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0079 others(2): Show |
12 | HG01109.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.983-529A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596627 | |||||||
| chr12:69596662 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-494G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596662 | |||||||
| chr12:69596664 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-492G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596664 | |||||||
| chr12:69596666 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-490T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596666 | |||||||
| chr12:69596667 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-489T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596667 | |||||||
| chr12:69596670 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-486C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596670 | |||||||
| chr12:69596671 | T | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(98): Show |
334 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.983-485T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596671 | |||||||
| chr12:69596672 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-484T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596672 | |||||||
| chr12:69596674 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-482T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596674 | |||||||
| chr12:69596675 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-481A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596675 | |||||||
| chr12:69596677 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-479G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596677 | |||||||
| chr12:69596679 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-477C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596679 | |||||||
| chr12:69596680 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-476A>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596680 | |||||||
| chr12:69596689 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-467C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596689 | |||||||
| chr12:69596691 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-465T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596691 | |||||||
| chr12:69596692 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-464G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596692 | |||||||
| chr12:69596693 | TCTTGTGC others(3): Show |
T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-462_983-453del others(10): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596693 | |||||||
| chr12:69596704 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-452G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596704 | |||||||
| chr12:69596709 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-447G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596709 | |||||||
| chr12:69596718 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-438G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596718 | |||||||
| chr12:69596721 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-435C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596721 | |||||||
| chr12:69596722 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-434T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596722 | |||||||
| chr12:69596723 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-433T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596723 | |||||||
| chr12:69596724 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-432A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596724 | |||||||
| chr12:69596726 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-430T>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596726 | |||||||
| chr12:69596728 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-428T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596728 | |||||||
| chr12:69596733 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-423G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596733 | |||||||
| chr12:69596734 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-422G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596734 | |||||||
| chr12:69596735 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-421T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596735 | |||||||
| chr12:69596736 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-420T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596736 | |||||||
| chr12:69596738 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-418G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596738 | |||||||
| chr12:69596740 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-416T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596740 | |||||||
| chr12:69596741 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.983-415T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596741 | |||||||
| chr12:69596800 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
372 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.983-356G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69596800 | |||||||
| chr12:69597042 | C | G | 1 | a0001c0002t0002g0024 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.983-114C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 10/15 | chr12 | 69597042 | |||||||
| chr12:69597304 | G | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0067 others(7): Show |
23 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1102+29G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 11/15 | chr12 | 69597304 | |||||||
| chr12:69597369 | T | G | 1 | a0001c0001t0001g0034 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1102+94T>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 11/15 | chr12 | 69597369 | |||||||
| chr12:69597439 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1102+164C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 11/15 | chr12 | 69597439 | |||||||
| chr12:69597788 | AAT | A | 20 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0009 others(17): Show |
76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1231+27_1231+28del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 69597788 | ||||||
| chr12:69597804 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1231+38C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597804 | |||||||
| chr12:69597818 | TAA | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0106 a0001c0001t0001g0109 |
4 | NA18947.hp1 NA18991.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231+53_1231+54del others(2): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597818 | |||||||
| chr12:69597842 | T | A | 1 | a0001c0001t0001g0017 | 5 | HG02040.hp2 HG02129.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231+76T>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597842 | |||||||
| chr12:69597847 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
371 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.1231+81C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597847 | |||||||
| chr12:69597880 | A | T | 20 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0009 others(17): Show |
76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1232-88A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597880 | |||||||
| chr12:69597895 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(22): Show |
105 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1232-73T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597895 | |||||||
| chr12:69597953 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1232-15A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 12/15 | chr12 | 69597953 | |||||||
| chr12:69598193 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0078 others(2): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1335+122G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 13/15 | chr12 | 69598193 | |||||||
| chr12:69598450 | G | GT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1435+31dupT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 69598450 | ||||||
| chr12:69598516 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1435+95C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598516 | |||||||
| chr12:69598521 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1435+100A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598521 | |||||||
| chr12:69598590 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0088 |
4 | NA18943.hp1 NA18968.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+169C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598590 | |||||||
| chr12:69598668 | G | A | 20 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0009 others(17): Show |
76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1435+247G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598668 | |||||||
| chr12:69598685 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(50): Show |
145 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1435+264A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598685 | |||||||
| chr12:69598739 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0119 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1435+318A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598739 | |||||||
| chr12:69598887 | T | TATCTACC others(5): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+467_1435+468i others(14): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 69598887 | ||||||
| chr12:69598889 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+468G>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598889 | |||||||
| chr12:69598891 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+470G>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598891 | |||||||
| chr12:69598893 | A | ATATCT | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+472_1435+473i others(7): Show |
CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598893 | |||||||
| chr12:69598894 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+473G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598894 | |||||||
| chr12:69598895 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
4 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+474T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598895 | |||||||
| chr12:69598940 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1435+519A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598940 | |||||||
| chr12:69598977 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1435+556G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598977 | |||||||
| chr12:69598978 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1435+557A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69598978 | |||||||
| chr12:69599037 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(18): Show |
98 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1435+616T>C | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599037 | |||||||
| chr12:69599256 | A | AT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1436-602dupT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 69599256 | ||||||
| chr12:69599307 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1436-556G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599307 | |||||||
| chr12:69599318 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0120 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1436-545A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599318 | |||||||
| chr12:69599357 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1436-506G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599357 | |||||||
| chr12:69599508 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
244 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(241): Show |
intron_variant | MODIFIER | c.1436-355C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599508 | |||||||
| chr12:69599555 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1436-308T>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599555 | |||||||
| chr12:69599575 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
7 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1436-288C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599575 | |||||||
| chr12:69599662 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1436-201C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599662 | |||||||
| chr12:69599721 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
244 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(241): Show |
intron_variant | MODIFIER | c.1436-142A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599721 | |||||||
| chr12:69599855 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.1436-8C>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 14/15 | chr12 | 69599855 | |||||||
| chr12:69600098 | A | G | 1 | a0001c0001t0001g0013 | 6 | HG00639.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1577+94A>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69600098 | |||||||
| chr12:69600253 | A | T | 1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1577+249A>T | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69600253 | |||||||
| chr12:69600476 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
14 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1577+472C>G | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69600476 | |||||||
| chr12:69600591 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
333 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.1577+596delT | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 69600591 | ||||||
| chr12:69600649 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1577+645G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69600649 | |||||||
| chr12:69600658 | T | TC | 21 | a0001c0002t0001g0064 a0001c0002t0002g0003 a0001c0002t0002g0006 others(18): Show |
77 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1578-631dupC | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 69600658 | ||||||
| chr12:69601152 | G | A | 1 | a0001c0002t0002g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1578-143G>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69601152 | |||||||
| chr12:69601259 | C | A | 20 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0009 others(17): Show |
76 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1578-36C>A | CCT2 | ENSG00000166226.13 | transcript | ENST00000299300.11 | protein_coding | 15/15 | chr12 | 69601259 |